A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066539



Internal ID19155758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1908976..1980774hg38UCSC Ensembl
Innerchr18:1908977..1980775hg19UCSC Ensembl
Innerchr18:1898977..1970775hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3871799
hg1971799
hg1871799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3311n100
Supporting Variantsnssv3564044, nssv3564042, nssv3564041, nssv3564045, nssv3564043
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)nsv1066539
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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