A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv975224



Internal ID16269180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144103155..144300921hg38UCSC Ensembl
Innerchr3:143821997..144019763hg19UCSC Ensembl
Innerchr3:145304687..145502453hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38197767
hg19197767
hg18197767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591925
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)nssv975224
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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