A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11194905



Internal ID4076420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156784730..156785355hg38UCSC Ensembl
Innerchr3:156784743..156785342hg38UCSC Ensembl
Outerchr3:156784717..156785368hg38UCSC Ensembl
chr3:156502519..156503144hg19UCSC Ensembl
Innerchr3:156502532..156503131hg19UCSC Ensembl
Outerchr3:156502506..156503157hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598306
Supporting Variants
SamplesHG03708
Known GenesLINC00886
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11194905
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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