A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061659



Internal ID19150878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60597209..60645984hg38UCSC Ensembl
Innerchr18:58264442..58313217hg19UCSC Ensembl
Innerchr18:56415422..56464197hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3848776
hg1948776
hg1848776
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3374n100
Supporting Variantsnssv3565613
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)nsv1061659
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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