A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4295



Internal ID15548990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:34742526..34842311hg38UCSC Ensembl
Outerchr4:34744148..34843933hg19UCSC Ensembl
Outerchr4:34420543..34520328hg18UCSC Ensembl
Outerchr4:34566714..34666499hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3899786
hg1999786
hg1899786
hg1799786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3249, nssv7073, nssv9391
SamplesNA12156, NA12878, NA18517
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)nsv4295
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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