A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002370



Internal ID15949640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:76560204..76600673hg38UCSC Ensembl
Innerchr4:77481357..77521826hg19UCSC Ensembl
Innerchr4:77700381..77740850hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3840470
hg1940470
hg1840470
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594696
Supporting Variants
Samples
Known GenesMIR4450, SHROOM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1002370
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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