A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4236



Internal ID15548925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:13056929..13089291hg38UCSC Ensembl
Outerchr4:13058553..13090915hg19UCSC Ensembl
Outerchr4:12667651..12700013hg18UCSC Ensembl
Outerchr4:12734822..12767184hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg387649
hg197649
hg187649
hg177649
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2452
SamplesNA18555
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)nsv4236
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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