A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596269



Internal ID16383678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:177643096..178226244hg38UCSC Ensembl
Innerchr4:178564250..179147398hg19UCSC Ensembl
Innerchr4:178801244..179384392hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38583149
hg19583149
hg18583149
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017036
Samples
Known GenesLINC01098, LINC01099
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596269
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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