A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067025



Internal ID19156244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1905345..2011934hg38UCSC Ensembl
Innerchr18:1905346..2011935hg19UCSC Ensembl
Innerchr18:1895346..2001935hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38106590
hg19106590
hg18106590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564021, nssv3564022
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)nsv1067025
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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