A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv985723



Internal ID16279679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193418687..193426029hg38UCSC Ensembl
Innerchr3:193136476..193143818hg19UCSC Ensembl
Innerchr3:194619170..194626512hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg387343
hg197343
hg187343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592946
Supporting Variants
Samples
Known GenesATP13A4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv985723
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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