A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4634



Internal ID15549363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183713904..183766388hg38UCSC Ensembl
Outerchr4:184635057..184687541hg19UCSC Ensembl
Outerchr4:184872051..184924535hg18UCSC Ensembl
Outerchr4:185010206..185062690hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3852485
hg1952485
hg1852485
hg1752485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4801, nssv7133
SamplesNA12156, NA19129
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)nsv4634
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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