A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071394



Internal ID18979078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60334538..60336639hg38UCSC Ensembl
chr17:58411899..58414000hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg382102
hg192102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762217
SamplesKWP1
Known GenesUSP32
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071394
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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