A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3328



Internal ID15538056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:10525742..10560077hg38UCSC Ensembl
Outerchr5:10525854..10560189hg19UCSC Ensembl
Outerchr5:10578854..10613189hg18UCSC Ensembl
Outerchr5:10578854..10613189hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg385405
hg195405
hg185405
hg175405
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4714
Supporting Variants
SamplesNA12878
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)nssv3328
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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