A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957912



Internal ID15905182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2452396..2454664hg38UCSC Ensembl
Innerchr3:2494080..2496348hg19UCSC Ensembl
Innerchr3:2469080..2471348hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg382269
hg192269
hg182269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589379
Supporting Variants
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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