A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5363



Internal ID15196431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:19038881..19068332hg38UCSC Ensembl
Outerchr1:19365375..19394826hg19UCSC Ensembl
Outerchr1:19237962..19267413hg18UCSC Ensembl
Outerchr1:19110681..19140132hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg385658
hg195658
hg185658
hg175658
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5298
Supporting Variants
SamplesNA19129
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv5363
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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