A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11039056



Internal ID666094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73687215..73688016hg38UCSC Ensembl
Innerchr3:73687215..73688016hg38UCSC Ensembl
Outerchr3:73686986..73688239hg38UCSC Ensembl
chr3:73736366..73737167hg19UCSC Ensembl
Innerchr3:73736366..73737167hg19UCSC Ensembl
Outerchr3:73736137..73737390hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596561
Supporting Variants
SamplesHG00309
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11039056
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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