A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068294



Internal ID18972987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23439270..23440071hg38UCSC Ensembl
chr10:23728199..23729000hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768672
SamplesKWP1
Known GenesOTUD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068294
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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