A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062465



Internal ID19151684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:57096597..57129427hg38UCSC Ensembl
Innerchr18:54763828..54796658hg19UCSC Ensembl
Innerchr18:52914826..52947656hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3832831
hg1932831
hg1832831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565461
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)nsv1062465
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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