A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577302



Internal ID16364711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67288152..67820837hg38UCSC Ensembl
Innerchr18:64955389..65488074hg19UCSC Ensembl
Innerchr18:63106369..63639054hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38532686
hg19532686
hg18532686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv886350
Samples
Known GenesDSEL, LOC643542
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577302
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