A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069953



Internal ID19317679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65321796..65323697hg38UCSC Ensembl
chr16:65355699..65357600hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764403
SamplesKWP1
Known GenesLINC00922
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069953
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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