A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069958



Internal ID18971721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96832142..96833143hg38UCSC Ensembl
chr10:98591899..98592900hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772644
SamplesKWP1
Known GenesLCOR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069958
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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