A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073836



Internal ID18969219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:474690..474934hg38UCSC Ensembl
chr5:474805..475049hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763260
SamplesKWP1
Known GenesSLC9A3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073836
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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