A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999082



Internal ID16945348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:42714903..42736802hg38UCSC Ensembl
Outerchr15:43007101..43029000hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3821900
hg1921900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952615
Supporting Variants
SamplesBILGI_BIOE
Known GenesCDAN1, STARD9
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999082
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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