A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7968



Internal ID15535896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:69046565..69080189hg38UCSC Ensembl
Outerchr4:69912283..69945907hg19UCSC Ensembl
Outerchr4:69946872..69980496hg18UCSC Ensembl
Outerchr4:70093043..70126667hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg385815
hg195815
hg185815
hg175815
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4373
Supporting Variants
SamplesNA12156
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)nssv7968
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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