A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959128



Internal ID15906398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12820109..12926604hg38UCSC Ensembl
Innerchr3:12861608..12968104hg19UCSC Ensembl
Innerchr3:12836608..12943104hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38106496
hg19106497
hg18106497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589716
Supporting Variants
Samples
Known GenesCAND2, IQSEC1, RPL32, SNORA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv959128
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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