A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1020491



Internal ID16314447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187776941..188150854hg38UCSC Ensembl
Innerchr4:188698095..189072008hg19UCSC Ensembl
Innerchr4:188935089..189309002hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38373914
hg19373914
hg18373914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596454
Supporting Variants
Samples
Known GenesTRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1020491
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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