A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766713



Internal ID18966157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31315980..31316270hg38UCSC Ensembl
chr16:31327301..31327591hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071284
Supporting Variants
SamplesKWP1
Known GenesITGAM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766713
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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