A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971966



Internal ID18882570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74927613..74927667hg38UCSC Ensembl
Outerchr15:75219954..75220008hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134471
Supporting Variants
SamplesKWS2
Known GenesCOX5A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971966
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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