A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638827



Internal ID7025612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63871574..63874047hg38UCSC Ensembl
Innerchr16:63871574..63874047hg38UCSC Ensembl
Outerchr16:63871322..63874239hg38UCSC Ensembl
chr16:63905478..63907951hg19UCSC Ensembl
Innerchr16:63905478..63907951hg19UCSC Ensembl
Outerchr16:63905226..63908143hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382474
hg192474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15498570, essv15498573, essv15498576, essv15498579, essv15498567, essv15498572, essv15498571, essv15498574, essv15498577, essv15498575, essv15498569, essv15498578, essv15498566, essv15498580, essv15498568
SamplesNA12286, HG01682, HG01284, HG00118, HG03781, HG01504, NA20765, NA21143, HG03238, NA20351, NA20289, NA19726, HG01105, HG01378, NA20585
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638827
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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