A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061326



Internal ID19150545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1907315..1980774hg38UCSC Ensembl
Innerchr18:1907316..1980775hg19UCSC Ensembl
Innerchr18:1897316..1970775hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3873460
hg1973460
hg1873460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3311n100
Supporting Variantsnssv3564035, nssv3564033, nssv3564032, nssv3564036, nssv3564039, nssv3564037, nssv3564028, nssv3564034, nssv3725264, nssv3564029, nssv3564031, nssv3564038, nssv3725263, nssv3564030
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)nsv1061326
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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