A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4351



Internal ID15549052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:57957211..57984555hg38UCSC Ensembl
Outerchr4:58823377..58850721hg19UCSC Ensembl
Outerchr4:58518134..58545478hg18UCSC Ensembl
Outerchr4:58664305..58691649hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385673
hg195673
hg185673
hg175673
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7960
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)nsv4351
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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