A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10977929



Internal ID2487305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32916889..32931494hg38UCSC Ensembl
Innerchr3:32916889..32931494hg38UCSC Ensembl
Outerchr3:32916389..32931994hg38UCSC Ensembl
chr3:32958381..32972986hg19UCSC Ensembl
Innerchr3:32958381..32972986hg19UCSC Ensembl
Outerchr3:32957881..32973486hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3814606
hg1914606
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595788
Supporting Variants
SamplesHG02187
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10977929
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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