A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10992



Internal ID15192894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:34239411..34252226hg38UCSC Ensembl
Outerchr19:34730316..34743131hg19UCSC Ensembl
Outerchr19:39422156..39434971hg18UCSC Ensembl
Outerchr19:39422156..39434971hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3810000
hg1910000
hg1810000
hg1710000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2468
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)nssv10992
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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