A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739357



Internal ID18690952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:40678818..40778347hg38UCSC Ensembl
Innerchr4:40680835..40780364hg19UCSC Ensembl
Innerchr4:40375592..40475121hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3899530
hg1999530
hg1899530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006924
Supporting Variants
Samples
Known GenesNSUN7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3739357
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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