A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962613



Internal ID15909883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:47449222..47450365hg38UCSC Ensembl
Innerchr3:47490712..47491855hg19UCSC Ensembl
Innerchr3:47465716..47466859hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381144
hg191144
hg181144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590214
Supporting Variants
Samples
Known GenesSCAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962613
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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