A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7999



Internal ID15535865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:121388928..121433956hg38UCSC Ensembl
Outerchr4:122310083..122355111hg19UCSC Ensembl
Outerchr4:122529533..122574561hg18UCSC Ensembl
Outerchr4:122667688..122712716hg17UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3845029
hg1945029
hg1845029
hg1745029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4495
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)nssv7999
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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