A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987688



Internal ID16281644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1278876..1318606hg38UCSC Ensembl
Innerchr4:1272664..1312394hg19UCSC Ensembl
Innerchr4:1262664..1302394hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3839731
hg1939731
hg1839731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593300
Supporting Variants
Samples
Known GenesMAEA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv987688
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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