A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153171



Internal ID15877271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148873132..148982830hg38UCSC Ensembl
Innerchr4:149794284..149903982hg19UCSC Ensembl
Innerchr4:150013734..150123432hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38109699
hg19109699
hg18109699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595686
Supporting Variants
SamplesHGDP00959
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153171
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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