A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637705



Internal ID6677806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4756306..4759820hg38UCSC Ensembl
Innerchr16:4756306..4759820hg38UCSC Ensembl
Outerchr16:4756065..4760150hg38UCSC Ensembl
chr16:4806307..4809821hg19UCSC Ensembl
Innerchr16:4806307..4809821hg19UCSC Ensembl
Outerchr16:4806066..4810151hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383515
hg193515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363808
SamplesNA18988
Known GenesZNF500
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637705
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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