A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672166



Internal ID15062132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65257915..65861834hg38UCSC Ensembl
Innerchr7:64720305..65326821hg19UCSC Ensembl
Innerchr7:64357740..64964256hg18UCSC Ensembl
Innerchr7:64164455..64770971hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38603920
hg19606517
hg18606517
hg17606517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517778
Supporting Variants
Samples
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, ZNF92
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672166
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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