A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702345



Internal ID15092311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76803016..77197121hg38UCSC Ensembl
Innerchr7:76432333..76826438hg19UCSC Ensembl
Innerchr7:76270269..76664374hg18UCSC Ensembl
Innerchr7:76076984..76471089hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38394106
hg19394106
hg18394106
hg17394106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526097
Supporting Variants
Samples
Known GenesCCDC146, DTX2P1-UPK3BP1-PMS2P11, FGL2, LOC100132832
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702345
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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