A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638722



Internal ID7025507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58169500..58171425hg38UCSC Ensembl
Innerchr16:58169500..58171425hg38UCSC Ensembl
Outerchr16:58169228..58171698hg38UCSC Ensembl
chr16:58203404..58205329hg19UCSC Ensembl
Innerchr16:58203404..58205329hg19UCSC Ensembl
Outerchr16:58203132..58205602hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381926
hg191926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15486799, essv15486790, essv15486802, essv15486800, essv15486801, essv15486791, essv15486796, essv15486789, essv15486788, essv15486798, essv15486795, essv15486794, essv15486792, essv15486797, essv15486793
SamplesHG03616, HG01686, NA12399, HG03754, HG03910, HG03132, HG01979, NA19774, HG00250, HG02219, HG01530, HG03720, HG03779, HG03600, NA12890
Known GenesCSNK2A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638722
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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