A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15372782



Internal ID6250712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9686238..9728984hg38UCSC Ensembl
Innerchr16:9686238..9728984hg38UCSC Ensembl
Outerchr16:9685738..9729484hg38UCSC Ensembl
chr16:9780095..9822841hg19UCSC Ensembl
Innerchr16:9780095..9822841hg19UCSC Ensembl
Outerchr16:9779595..9823341hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3842747
hg1942747
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637875
Supporting Variants
SamplesNA19776
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15372782
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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