A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv971725



Internal ID16265681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119632803..119635586hg38UCSC Ensembl
Innerchr3:119351650..119354433hg19UCSC Ensembl
Innerchr3:120834340..120837123hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382784
hg192784
hg182784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591374
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)nssv971725
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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