A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9335



Internal ID15193600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:38742055..38788553hg38UCSC Ensembl
Outerchr19:39232695..39279193hg19UCSC Ensembl
Outerchr19:43924535..43971033hg18UCSC Ensembl
Outerchr19:43924535..43971033hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3846499
hg1946499
hg1846499
hg1746499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7307
Supporting Variants
SamplesNA18517
Known GenesCAPN12, LGALS7
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)nssv9335
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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