A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064182



Internal ID19153401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39636758..39682665hg38UCSC Ensembl
Innerchr18:37216722..37262629hg19UCSC Ensembl
Innerchr18:35470720..35516627hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3845908
hg1945908
hg1845908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3338n100
Supporting Variantsnssv3564219
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)nsv1064182
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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