A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15441654



Internal ID5443470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29545957..29566985hg38UCSC Ensembl
Innerchr16:29545957..29566985hg38UCSC Ensembl
Outerchr16:29545457..29567485hg38UCSC Ensembl
chr16:29557278..29578306hg19UCSC Ensembl
Innerchr16:29557278..29578306hg19UCSC Ensembl
Outerchr16:29556778..29578806hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3821029
hg1921029
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638365
Supporting Variants
SamplesHG01896
Known GenesLOC440354
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15441654
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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