A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765862



Internal ID19308000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48608588..48610689hg38UCSC Ensembl
chr16:48642499..48644600hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg382102
hg192102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071288
Supporting Variants
SamplesKWP1
Known GenesN4BP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765862
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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