A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068657



Internal ID18977080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1699405..1701706hg38UCSC Ensembl
chr10:1741599..1743900hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg382302
hg192302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764932
SamplesKWP1
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068657
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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