A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762178



Internal ID19312594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55761187..55788788hg38UCSC Ensembl
chr16:55795099..55822700hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3827602
hg1927602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069947
Supporting Variants
SamplesKWP1
Known GenesCES1P1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762178
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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