A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7305



Internal ID15205615
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5727, nssv1436
SamplesNA19129, NA19240
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)nsv7305
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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