A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009659



Internal ID19098877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39757984..39801886hg38UCSC Ensembl
Innerchr4:39759604..39803506hg19UCSC Ensembl
Innerchr4:39435999..39479901hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3843903
hg1943903
hg1843903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5193n100
Supporting Variantsnssv3625035
Samples
Known GenesUBE2K
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009659
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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