A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15378626



Internal ID2982323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14055686..14063877hg38UCSC Ensembl
Innerchr16:14055686..14063877hg38UCSC Ensembl
Outerchr16:14055447..14064026hg38UCSC Ensembl
chr16:14149543..14157734hg19UCSC Ensembl
Innerchr16:14149543..14157734hg19UCSC Ensembl
Outerchr16:14149304..14157883hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg388192
hg198192
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637995
Supporting Variants
SamplesHG02634
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15378626
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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