A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638935



Internal ID7025720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69820414..69824905hg38UCSC Ensembl
Innerchr16:69820414..69824905hg38UCSC Ensembl
Outerchr16:69819955..69825073hg38UCSC Ensembl
chr16:69854317..69858808hg19UCSC Ensembl
Innerchr16:69854317..69858808hg19UCSC Ensembl
Outerchr16:69853858..69858976hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg384492
hg194492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15503808, essv15503807, essv15503809, essv15503813, essv15503806, essv15503812, essv15503805, essv15503810, essv15503811
SamplesHG01060, HG02690, NA19917, HG03709, HG02102, HG00140, HG03634, HG01858, HG04219
Known GenesWWP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638935
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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