A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7133



Internal ID15536731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183713904..183741542hg38UCSC Ensembl
Outerchr4:184635057..184662695hg19UCSC Ensembl
Outerchr4:184872051..184899689hg18UCSC Ensembl
Outerchr4:185010206..185037844hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3827639
hg1927639
hg1827639
hg1727639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4634
Supporting Variants
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)nssv7133
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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