A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9795



Internal ID15539853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45737081..45773275hg38UCSC Ensembl
Outerchr10:46232529..46268723hg19UCSC Ensembl
Outerchr10:45552535..45588729hg18UCSC Ensembl
Outerchr10:45552535..45588729hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3836195
hg1936195
hg1836195
hg1736195
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7202
Supporting Variants
SamplesNA18507
Known GenesFAM21C
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)nssv9795
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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