A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576797



Internal ID16364206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:44397788..44400903hg38UCSC Ensembl
Innerchr18:41977753..41980868hg19UCSC Ensembl
Innerchr18:40231751..40234866hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg383116
hg193116
hg183116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5913n54
Supporting Variantsnssv882597
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576797
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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