A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952079



Internal ID16954266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89685593..89749492hg38UCSC Ensembl
Outerchr16:89752001..89815900hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3863900
hg1963900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000198
SamplesBILGI_BIOE
Known GenesCDK10, FANCA, SPATA2L, VPS9D1, VPS9D1-AS1, ZNF276
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952079
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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