A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997905



Internal ID19157441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5414387..5503363hg38UCSC Ensembl
Innerchr4:5416114..5505090hg19UCSC Ensembl
Innerchr4:5467015..5555991hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3888977
hg1988977
hg1888977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3738143
Samples
Known GenesSTK32B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997905
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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