A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069440



Internal ID18969988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1616427..1616618hg38UCSC Ensembl
chr10:1658622..1658813hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770026
SamplesKWP1
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069440
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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