A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634342



Internal ID6674460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45126285..45128141hg38UCSC Ensembl
Innerchr14:45126285..45128141hg38UCSC Ensembl
Outerchr14:45125983..45128479hg38UCSC Ensembl
chr14:45595488..45597344hg19UCSC Ensembl
Innerchr14:45595488..45597344hg19UCSC Ensembl
Outerchr14:45595186..45597682hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg381857
hg191857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15002582, essv15002565, essv15002589, essv15002580, essv15002567, essv15002596, essv15002566, essv15002569, essv15002573, essv15002568, essv15002588, essv15002595, essv15002592, essv15002579, essv15002575, essv15002591, essv15002597, essv15002570, essv15002587, essv15002562, essv15002585, essv15002586, essv15002574, essv15002594, essv15002577, essv15002571, essv15002584, essv15002564, essv15002578, essv15002581, essv15002583, essv15002593, essv15002563, essv15002590, essv15002572, essv15002576
SamplesHG00608, NA18647, HG02122, NA18603, NA18596, HG02356, HG00622, HG02151, NA18982, NA18619, HG00610, HG01859, HG00632, HG02067, NA18985, NA18954, HG00596, HG04195, HG01810, HG01852, HG02604, NA18963, NA18542, NA18543, HG00565, HG01800, HG02137, NA19078, HG02113, HG01872, NA19011, NA19004, NA18623, NA19063, NA18740, HG03931
Known GenesFKBP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634342
Frequency
Sample Size2504
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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