A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525729



Internal ID15106336
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 StatusM
Merged Variants
Supporting Variantsnssv701893
Samples
Known GenesPOT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525729
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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