A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061152



Internal ID19150371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14726147..14753436hg38UCSC Ensembl
Innerchr18:14726146..14753435hg19UCSC Ensembl
Innerchr18:14716146..14743435hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3827290
hg1927290
hg1827290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564122
Samples
Known GenesANKRD30B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061152
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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