A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573739



Internal ID16014462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89625890..89696855hg38UCSC Ensembl
Innerchr16:89692298..89763263hg19UCSC Ensembl
Innerchr16:88219799..88290764hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3870966
hg1970966
hg1870966
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863335
Samples
Known GenesCDK10, CHMP1A, DPEP1, SPATA2L, SPATA33
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573739
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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