A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065881



Internal ID19155100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:38970121..39098891hg38UCSC Ensembl
Innerchr18:36550085..36678855hg19UCSC Ensembl
Innerchr18:34804083..34932853hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38128771
hg19128771
hg18128771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564215
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)nsv1065881
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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