A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636683



Internal ID7023477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61394751..61406619hg38UCSC Ensembl
Innerchr15:61394751..61406619hg38UCSC Ensembl
Outerchr15:61394545..61406830hg38UCSC Ensembl
chr15:61686950..61698818hg19UCSC Ensembl
Innerchr15:61686950..61698818hg19UCSC Ensembl
Outerchr15:61686744..61699029hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3811869
hg1911869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15264561, essv15264586, essv15264569, essv15264590, essv15264580, essv15264577, essv15264587, essv15264571, essv15264564, essv15264563, essv15264576, essv15264573, essv15264585, essv15264591, essv15264583, essv15264579, essv15264594, essv15264575, essv15264565, essv15264568, essv15264574, essv15264592, essv15264582, essv15264578, essv15264584, essv15264589, essv15264570, essv15264562, essv15264593, essv15264581, essv15264567, essv15264588, essv15264559, essv15264595, essv15264566, essv15264572, essv15264560
SamplesHG01485, NA12842, HG00361, HG01066, NA12045, HG00103, HG00364, NA20332, NA12399, HG01766, NA20756, NA20822, HG00311, HG00379, HG01495, HG01281, HG01259, HG00178, NA20885, NA20809, HG04195, HG03781, HG01607, NA20525, HG00250, NA11893, NA11894, HG00117, HG02283, NA20534, NA12873, NA12046, NA20516, HG01432, HG00267, HG04171, HG01378
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636683
Frequency
Sample Size2504
Observed Gain0
Observed Loss37
Observed Complex0
Frequencyn/a


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