A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704885



Internal ID15441537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:134712332..134714924hg38UCSC Ensembl
Innerchr3:134431174..134433766hg19UCSC Ensembl
Innerchr3:135913864..135916456hg18UCSC Ensembl
Innerchr3:135913872..135916464hg17UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg382593
hg192593
hg182593
hg172593
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528307
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704885
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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