A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020622



Internal ID19109841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65696391..65874892hg38UCSC Ensembl
Innerchr7:65161364..65339879hg19UCSC Ensembl
Innerchr7:64798799..64977314hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38178502
hg19178516
hg18178516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655624, nssv3655623
Samples
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, VKORC1L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020622
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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