A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967772



Internal ID16261728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:93989976..94060820hg38UCSC Ensembl
Innerchr3:93708820..93779664hg19UCSC Ensembl
Innerchr3:95191510..95262354hg18UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg3870845
hg1970845
hg1870845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590987
Supporting Variants
Samples
Known GenesARL13B, DHFRL1, STX19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv967772
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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