A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132874



Internal ID18910277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:85004684..85004744hg38UCSC Ensembl
Outerchr16:85038290..85038350hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987668
SamplesKWS1
Known GenesZDHHC7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132874
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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