A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636800



Internal ID6676907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68059508..68060467hg38UCSC Ensembl
Innerchr15:68059536..68060439hg38UCSC Ensembl
Outerchr15:68059480..68060495hg38UCSC Ensembl
chr15:68351846..68352805hg19UCSC Ensembl
Innerchr15:68351874..68352777hg19UCSC Ensembl
Outerchr15:68351818..68352833hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15279384, essv15279383, essv15279386, essv15279391, essv15279390, essv15279385, essv15279389, essv15279382, essv15279381, essv15279387, essv15279388
SamplesHG02890, NA19399, NA18881, HG01170, NA19036, NA19456, HG02817, HG02594, NA20357, NA19376, HG02861
Known GenesPIAS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636800
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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