A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658236



Internal ID15394888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13788122..13817610hg38UCSC Ensembl
Innerchr7:13827747..13857235hg19UCSC Ensembl
Innerchr7:13794272..13823760hg18UCSC Ensembl
Innerchr7:13600987..13630475hg17UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3829489
hg1929489
hg1829489
hg1729489
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519601
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658236
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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