A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060753



Internal ID19149972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:41089926..41101803hg38UCSC Ensembl
Innerchr18:38669890..38681767hg19UCSC Ensembl
Innerchr18:36923888..36935765hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3811878
hg1911878
hg1811878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565342
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)nsv1060753
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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