A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696708



Internal ID15086674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:130363646..130387196hg38UCSC Ensembl
Innerchr7:130003487..130027037hg19UCSC Ensembl
Innerchr7:129790723..129814273hg18UCSC Ensembl
Innerchr7:129597438..129620988hg17UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3823551
hg1923551
hg1823551
hg1723551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515945
Supporting Variants
Samples
Known GenesCPA1, CPA5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696708
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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