A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11073



Internal ID15539635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:193148605..193174225hg38UCSC Ensembl
Outerchr3:192866394..192892014hg19UCSC Ensembl
Outerchr3:194349088..194374708hg18UCSC Ensembl
Outerchr3:194349096..194374716hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3825621
hg1925621
hg1825621
hg1725621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4174
Supporting Variants
SamplesNA15510
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)nssv11073
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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