A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10975040



Internal ID976856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32297309..32298230hg38UCSC Ensembl
Innerchr3:32297342..32298197hg38UCSC Ensembl
Outerchr3:32297276..32298263hg38UCSC Ensembl
chr3:32338801..32339722hg19UCSC Ensembl
Innerchr3:32338834..32339689hg19UCSC Ensembl
Outerchr3:32338768..32339755hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38922
hg19922
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595770
Supporting Variants
SamplesNA20502
Known GenesCMTM8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10975040
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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