A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4535



Internal ID15549254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:145992631..146030801hg38UCSC Ensembl
Outerchr4:146913783..146951953hg19UCSC Ensembl
Outerchr4:147133233..147171403hg18UCSC Ensembl
Outerchr4:147271388..147309558hg17UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3838171
hg1938171
hg1838171
hg1738171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4784, nssv7122
SamplesNA12156, NA19129
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)nsv4535
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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