A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009645



Internal ID19098863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:23650835..23707992hg38UCSC Ensembl
Innerchr4:23652458..23709615hg19UCSC Ensembl
Innerchr4:23261556..23318713hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3857158
hg1957158
hg1857158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5156n100
Supporting Variantsnssv3620586
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009645
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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