A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701501



Internal ID15091467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72631705..72657233hg38UCSC Ensembl
Innerchr7:72096690..72122218hg19UCSC Ensembl
Innerchr7:71734626..71760154hg18UCSC Ensembl
Innerchr7:71541341..71566869hg17UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3825529
hg1925529
hg1825529
hg1725529
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520573
Supporting Variants
Samples
Known GenesTYW1B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701501
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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