A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573741



Internal ID16014464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89647732..89648410hg38UCSC Ensembl
Innerchr16:89714140..89714818hg19UCSC Ensembl
Innerchr16:88241641..88242319hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38679
hg19679
hg18679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5323n54
Supporting Variantsnssv863338
Samples
Known GenesCHMP1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573741
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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