A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1017036



Internal ID16310992
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 StatusS
Merged Variantsnsv596269
Supporting Variants
Samples
Known GenesLINC01098, LINC01099
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1017036
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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