A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv974757



Internal ID16268713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136302814..136307088hg38UCSC Ensembl
Innerchr3:136021656..136025930hg19UCSC Ensembl
Innerchr3:137504346..137508620hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg384275
hg194275
hg184275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591842
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)nssv974757
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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