A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069965



Internal ID18980075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112455140..112455541hg38UCSC Ensembl
chr10:114214899..114215300hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772925
SamplesKWP1
Known GenesVTI1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069965
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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