A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034883



Internal ID18777415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5612049..5656516hg38UCSC Ensembl
Innerchr7:5651680..5696147hg19UCSC Ensembl
Innerchr7:5618206..5662673hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3844468
hg1944468
hg1844468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655058
Samples
Known GenesRNF216
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034883
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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