A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577057



Internal ID16364466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59990010..60028812hg38UCSC Ensembl
Innerchr18:57657242..57696044hg19UCSC Ensembl
Innerchr18:55808222..55847024hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3838803
hg1938803
hg1838803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv884914
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577057
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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