A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076153



Internal ID18977016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15523904..15526405hg38UCSC Ensembl
chr1:15850399..15852900hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763981
SamplesKWP1
Known GenesCASP9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076153
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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