A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765213



Internal ID18964762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50085902..50087303hg38UCSC Ensembl
chr15:50378099..50379500hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070697
Supporting Variants
SamplesKWP1
Known GenesATP8B4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765213
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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