A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6803



Internal ID15190375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:55768393..55773041hg38UCSC Ensembl
Outerchr19:56279759..56284407hg19UCSC Ensembl
Outerchr19:60971571..60976219hg18UCSC Ensembl
Outerchr19:60971571..60976219hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg389648
hg199648
hg189648
hg179648
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2556
Supporting Variants
SamplesNA12156
Known GenesRFPL4AL1
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)nssv6803
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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