A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1890



Internal ID15541173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37070260..37107822hg38UCSC Ensembl
Outerchr10:37359188..37396750hg19UCSC Ensembl
Outerchr10:37399194..37436756hg18UCSC Ensembl
Outerchr10:37399194..37436756hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3837563
hg1937563
hg1837563
hg1737563
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7201
Supporting Variants
SamplesNA18555
Known Genes
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)nssv1890
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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