A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664934



Internal ID15054900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76556311..76914772hg38UCSC Ensembl
Innerchr7:76185628..76544089hg19UCSC Ensembl
Innerchr7:76023564..76382025hg18UCSC Ensembl
Innerchr7:75830279..76188740hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38358462
hg19358462
hg18358462
hg17358462
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)nssv664934
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer