A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063581



Internal ID19152800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39636758..39693083hg38UCSC Ensembl
Innerchr18:37216722..37273047hg19UCSC Ensembl
Innerchr18:35470720..35527045hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3856326
hg1956326
hg1856326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3338n100
Supporting Variantsnssv3564220
Samples
Known GenesLINC00669, MIR5583-1, MIR5583-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063581
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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