A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764422



Internal ID19315178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24871752..24872653hg38UCSC Ensembl
chr15:25116899..25117800hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069842
Supporting Variants
SamplesKWP1
Known GenesSNRPN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764422
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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