A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7073



Internal ID15536791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:34759410..34842311hg38UCSC Ensembl
Outerchr4:34761032..34843933hg19UCSC Ensembl
Outerchr4:34437427..34520328hg18UCSC Ensembl
Outerchr4:34583598..34666499hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3882902
hg1982902
hg1882902
hg1782902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4295
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)nssv7073
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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