A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7111



Internal ID15190067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:106116666..106157319hg38UCSC Ensembl
Outerchr4:107037823..107078476hg19UCSC Ensembl
Outerchr4:107257272..107297925hg18UCSC Ensembl
Outerchr4:107395427..107436080hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3840654
hg1940654
hg1840654
hg1740654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4450
Supporting Variants
SamplesNA12156
Known GenesTBCK
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)nssv7111
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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