A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638376



Internal ID7025162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29937973..29948907hg38UCSC Ensembl
Innerchr16:29938473..29948407hg38UCSC Ensembl
Outerchr16:29936973..29949907hg38UCSC Ensembl
chr16:29949294..29960228hg19UCSC Ensembl
Innerchr16:29949794..29959728hg19UCSC Ensembl
Outerchr16:29948294..29961228hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3810935
hg1910935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15441736, essv15441737, essv15441734, essv15441733, essv15441735, essv15441732
SamplesHG02325, HG03311, HG03391, HG01890, HG03240, HG03025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638376
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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