A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639606



Internal ID7026385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:90020213..90097271hg38UCSC Ensembl
Innerchr16:90020363..90097121hg38UCSC Ensembl
Outerchr16:90020063..90097421hg38UCSC Ensembl
chr16:90086621..90163679hg19UCSC Ensembl
Innerchr16:90086771..90163529hg19UCSC Ensembl
Outerchr16:90086471..90163829hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3877059
hg1977059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15569969, essv15569968, essv15569966, essv15569967
SamplesHG02610, HG02624, HG02595, HG02461
Known GenesC16orf3, GAS8, PRDM7, URAHP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639606
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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