A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15514796



Internal ID5660586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71800111..71805785hg38UCSC Ensembl
Innerchr16:71800113..71805784hg38UCSC Ensembl
Outerchr16:71800110..71805787hg38UCSC Ensembl
chr16:71834014..71839688hg19UCSC Ensembl
Innerchr16:71834016..71839687hg19UCSC Ensembl
Outerchr16:71834013..71839690hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg385675
hg195675
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638978
Supporting Variants
SamplesNA19072
Known GenesAP1G1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15514796
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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