A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576453



Internal ID16017176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9913348..9914777hg38UCSC Ensembl
Innerchr18:9913345..9914774hg19UCSC Ensembl
Innerchr18:9903345..9904774hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381430
hg191430
hg181430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878074
Samples
Known GenesVAPA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576453
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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