A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772653



Internal ID19312825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74360601..74428802hg38UCSC Ensembl
chr16:74394499..74462700hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3868202
hg1968202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076436
Supporting Variants
SamplesKWP1
Known GenesCLEC18B, LOC283922
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772653
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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