A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4174



Internal ID15548857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:193144139..193177091hg38UCSC Ensembl
Outerchr3:192861928..192894880hg19UCSC Ensembl
Outerchr3:194344622..194377574hg18UCSC Ensembl
Outerchr3:194344630..194377582hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3832953
hg1932953
hg1832953
hg1732953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7056, nssv359, nssv4707, nssv11073, nssv3222
SamplesNA12156, NA12878, NA15510, NA19240, 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)nsv4174
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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