A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv974759



Internal ID16268715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136302814..136307191hg38UCSC Ensembl
Innerchr3:136021656..136026033hg19UCSC Ensembl
Innerchr3:137504346..137508723hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg384378
hg194378
hg184378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591843
Supporting Variants
Samples
Known GenesPCCB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv974759
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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