A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10997



Internal ID15192899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39882937..39899159hg38UCSC Ensembl
Outerchr19:40373577..40389255hg19UCSC Ensembl
Outerchr19:45065417..45081095hg18UCSC Ensembl
Outerchr19:45065417..45081095hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3816223
hg1915679
hg1815679
hg1715679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2483
Supporting Variants
SamplesNA15510
Known GenesFCGBP
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)nssv10997
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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