A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666884



Internal ID15056850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76556311..76880902hg38UCSC Ensembl
Innerchr7:76185628..76510219hg19UCSC Ensembl
Innerchr7:76023564..76348155hg18UCSC Ensembl
Innerchr7:75830279..76154870hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38324592
hg19324592
hg18324592
hg17324592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517634
Supporting Variants
Samples
Known GenesLOC100133091, POMZP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666884
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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