A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762160



Internal ID18964262
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 StatusS
Merged Variantsnsv1069918
Supporting Variants
SamplesKWP1
Known GenesCIITA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762160
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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