A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055221



Internal ID19144440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1355677..1616028hg38UCSC Ensembl
Innerchr18:1355678..1616029hg19UCSC Ensembl
Innerchr18:1345678..1606029hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38260352
hg19260352
hg18260352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563901
Samples
Known GenesLINC00470
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055221
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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