A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4405



Internal ID15549111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:84352186..84374056hg38UCSC Ensembl
Outerchr4:85273339..85295209hg19UCSC Ensembl
Outerchr4:85492363..85514233hg18UCSC Ensembl
Outerchr4:85630518..85652388hg17UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg388093
hg198093
hg188093
hg178093
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10410
SamplesNA18956
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)nsv4405
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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