A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056480



Internal ID18799011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:56980170..57097183hg38UCSC Ensembl
Innerchr18:54647401..54764414hg19UCSC Ensembl
Innerchr18:52798399..52915412hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38117014
hg19117014
hg18117014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565460
Samples
Known GenesLINC-ROR, WDR7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056480
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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