A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1436



Internal ID15197585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:10969796..11006396hg38UCSC Ensembl
Outerchr19:11080472..11117072hg19UCSC Ensembl
Outerchr19:10941472..10978072hg18UCSC Ensembl
Outerchr19:10941472..10978072hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3836601
hg1936601
hg1836601
hg1736601
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7305
Supporting Variants
SamplesNA19240
Known GenesSMARCA4
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)nssv1436
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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