A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv991227



Internal ID15938497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7970145..7973020hg38UCSC Ensembl
Innerchr4:7971872..7974747hg19UCSC Ensembl
Innerchr4:8022772..8025647hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg382876
hg192876
hg182876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593622
Supporting Variants
Samples
Known GenesABLIM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv991227
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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