A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658995



Internal ID15395647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:135716655..135739062hg38UCSC Ensembl
Innerchr3:135435497..135457904hg19UCSC Ensembl
Innerchr3:136918187..136940594hg18UCSC Ensembl
Innerchr3:136918195..136940602hg17UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3822408
hg1922408
hg1822408
hg1722408
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515820
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658995
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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