A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637840



Internal ID6677940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8681580..8692924hg38UCSC Ensembl
Innerchr16:8681730..8692774hg38UCSC Ensembl
Outerchr16:8681430..8693074hg38UCSC Ensembl
chr16:8775437..8786781hg19UCSC Ensembl
Innerchr16:8775587..8786631hg19UCSC Ensembl
Outerchr16:8775287..8786931hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3811345
hg1911345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15371916, essv15371917
SamplesHG04210, HG03643
Known GenesABAT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637840
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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