A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068264



Internal ID18976904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1292969..1293037hg38UCSC Ensembl
chr10:1335164..1335232hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767330
SamplesKWP1
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068264
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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