A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701893



Internal ID15091859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124897982..124909519hg38UCSC Ensembl
Innerchr7:124538036..124549573hg19UCSC Ensembl
Innerchr7:124325272..124336809hg18UCSC Ensembl
Innerchr7:124131987..124143524hg17UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3811538
hg1911538
hg1811538
hg1711538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525729
Supporting Variants
Samples
Known GenesPOT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701893
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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