A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10186



Internal ID15195926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:38730589..38790606hg38UCSC Ensembl
Outerchr19:39221229..39281246hg19UCSC Ensembl
Outerchr19:43913069..43973086hg18UCSC Ensembl
Outerchr19:43913069..43973086hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3860018
hg1960018
hg1860018
hg1760018
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7307
Supporting Variants
SamplesNA18956
Known GenesCAPN12, LGALS7, LGALS7B
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)nssv10186
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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