A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064627



Internal ID19153846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1900056..1980774hg38UCSC Ensembl
Innerchr18:1900057..1980775hg19UCSC Ensembl
Innerchr18:1890057..1970775hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg3880719
hg1980719
hg1880719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3311n100
Supporting Variantsnssv3563959
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)nsv1064627
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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