A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069918



Internal ID18977582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10910972..10911032hg38UCSC Ensembl
chr16:11004829..11004889hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762160
SamplesKWP1
Known GenesCIITA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069918
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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