A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9396



Internal ID15540347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:74703836..74735823hg38UCSC Ensembl
Outerchr4:75629047..75661033hg19UCSC Ensembl
Outerchr4:75848071..75880057hg18UCSC Ensembl
Outerchr4:75986226..76018212hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3831988
hg1931987
hg1831987
hg1731987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4390
Supporting Variants
SamplesNA18517
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)nssv9396
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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