A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9401



Internal ID15540352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:147270792..147296672hg38UCSC Ensembl
Outerchr4:148191944..148217824hg19UCSC Ensembl
Outerchr4:148411394..148437274hg18UCSC Ensembl
Outerchr4:148549549..148575429hg17UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3811696
hg1911696
hg1811696
hg1711696
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4539
Supporting Variants
SamplesNA18517
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)nssv9401
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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