A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694815



Internal ID15084781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180183107..180190519hg38UCSC Ensembl
Innerchr1:180152242..180159654hg19UCSC Ensembl
Innerchr1:178418865..178426277hg18UCSC Ensembl
Innerchr1:176883899..176891311hg17UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg387413
hg197413
hg187413
hg177413
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522045
Supporting Variants
Samples
Known GenesQSOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694815
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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