A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577031



Internal ID16364440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:57508517..57542169hg38UCSC Ensembl
Innerchr18:55175749..55209401hg19UCSC Ensembl
Innerchr18:53326747..53360399hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3833653
hg1933653
hg1833653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv884853
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577031
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