A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695189



Internal ID15085155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:934152..935131hg38UCSC Ensembl
Innerchr3:975836..976815hg19UCSC Ensembl
Innerchr3:950836..951815hg18UCSC Ensembl
Innerchr3:950836..951815hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38980
hg19980
hg18980
hg17980
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517343
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695189
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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