A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657754



Internal ID15047720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76803016..77008124hg38UCSC Ensembl
Innerchr7:76432333..76637441hg19UCSC Ensembl
Innerchr7:76270269..76475377hg18UCSC Ensembl
Innerchr7:76076984..76282092hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38205109
hg19205109
hg18205109
hg17205109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517634
Supporting Variants
Samples
Known GenesDTX2P1-UPK3BP1-PMS2P11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657754
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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