A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026581



Internal ID19115799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155953171..155964024hg38UCSC Ensembl
Innerchr4:156874323..156885176hg19UCSC Ensembl
Innerchr4:157093773..157104626hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3810854
hg1910854
hg1810854
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636134, nssv3636135
Samples
Known GenesCTSO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026581
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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