A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655058



Internal ID18606653
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 StatusS
Merged Variantsnsv1034883
Supporting Variants
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)nssv3655058
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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