A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763249



Internal ID18960351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89919991..89925792hg38UCSC Ensembl
chr16:89986399..89992200hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg385802
hg195802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070371
Supporting Variants
SamplesKWP1
Known GenesMC1R, TUBB3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763249
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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