A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576629



Internal ID16364038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:30529743..30562809hg38UCSC Ensembl
Innerchr18:28109709..28142775hg19UCSC Ensembl
Innerchr18:26363707..26396773hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3833067
hg1933067
hg1833067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878939
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576629
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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