A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576588



Internal ID16363997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26991709..26992925hg38UCSC Ensembl
Innerchr18:24571673..24572889hg19UCSC Ensembl
Innerchr18:22825671..22826887hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381217
hg191217
hg181217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878864
Samples
Known GenesCHST9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576588
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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