A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576939



Internal ID16364348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:53038889..53135803hg38UCSC Ensembl
Innerchr18:50565259..50662173hg19UCSC Ensembl
Innerchr18:48819257..48916171hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3896915
hg1996915
hg1896915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv883301
Samples
Known GenesDCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576939
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer