A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701779



Internal ID15091745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:130383698..130387196hg38UCSC Ensembl
Innerchr7:130023539..130027037hg19UCSC Ensembl
Innerchr7:129810775..129814273hg18UCSC Ensembl
Innerchr7:129617490..129620988hg17UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg383499
hg193499
hg183499
hg173499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515945
Supporting Variants
Samples
Known GenesCPA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701779
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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