A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020103



Internal ID18762639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5754589..5854324hg38UCSC Ensembl
Innerchr7:5794220..5893955hg19UCSC Ensembl
Innerchr7:5760746..5860481hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3899736
hg1999736
hg1899736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655064
Samples
Known GenesRNF216, ZNF815P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020103
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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