A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1082348



Internal ID15935534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31548004..31551836hg38UCSC Ensembl
Innerchr7:31587618..31591450hg19UCSC Ensembl
Innerchr7:31554143..31557975hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg383833
hg193833
hg183833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606550
Supporting Variants
Samples
Known GenesCCDC129
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1082348
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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