A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118354



Internal ID19259620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:55762388..55788588hg38UCSC Ensembl
Outerchr16:55796300..55822500hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3826201
hg1926201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981035
SamplesKWS1
Known GenesCES1P1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118354
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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