A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958020



Internal ID15905290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4051238..4059672hg38UCSC Ensembl
Innerchr3:4092922..4101356hg19UCSC Ensembl
Innerchr3:4067922..4076356hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg388435
hg198435
hg188435
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589421
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv958020
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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