A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674261



Internal ID15064227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76556311..76927895hg38UCSC Ensembl
Innerchr7:76185628..76557212hg19UCSC Ensembl
Innerchr7:76023564..76395148hg18UCSC Ensembl
Innerchr7:75830279..76201863hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38371585
hg19371585
hg18371585
hg17371585
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)nssv674261
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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