A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15373025



Internal ID5374841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10448860..10451013hg38UCSC Ensembl
Innerchr16:10448885..10450989hg38UCSC Ensembl
Outerchr16:10448836..10451038hg38UCSC Ensembl
chr16:10542717..10544870hg19UCSC Ensembl
Innerchr16:10542742..10544846hg19UCSC Ensembl
Outerchr16:10542693..10544895hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637900
Supporting Variants
SamplesHG03934
Known GenesATF7IP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15373025
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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