A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689209



Internal ID15079175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76430244..76920728hg38UCSC Ensembl
Innerchr7:76059561..76550045hg19UCSC Ensembl
Innerchr7:75897497..76387981hg18UCSC Ensembl
Innerchr7:75704212..76194696hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38490485
hg19490485
hg18490485
hg17490485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517634
Supporting Variants
Samples
Known GenesDTX2, FDPSP2, LOC100133091, POMZP3, UPK3B, ZP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689209
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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