A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv986822



Internal ID16280778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195698774..195714541hg38UCSC Ensembl
Innerchr3:195425645..195441412hg19UCSC Ensembl
Innerchr3:196910825..196927083hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3815768
hg1915768
hg1816259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593036
Supporting Variants
Samples
Known GenesMIR570
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv986822
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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