A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4635



Internal ID15202678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183805526..183850378hg38UCSC Ensembl
Outerchr4:184726679..184771531hg19UCSC Ensembl
Outerchr4:184963673..185008525hg18UCSC Ensembl
Outerchr4:185101828..185146680hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3844853
hg1944853
hg1844853
hg1744853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8041
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)nsv4635
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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