A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4330



Internal ID15549029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:48931019..48956104hg38UCSC Ensembl
Outerchr4:48933036..48958121hg19UCSC Ensembl
Outerchr4:48627793..48652878hg18UCSC Ensembl
Outerchr4:48773964..48799049hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3825086
hg1925086
hg1825086
hg1725086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7952
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)nsv4330
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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