A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9801



Internal ID15539861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:87303527..87400529hg38UCSC Ensembl
Outerchr10:89063284..89160286hg19UCSC Ensembl
Outerchr10:89053264..89150266hg18UCSC Ensembl
Outerchr10:89053264..89150266hg17UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3897003
hg1997003
hg1897003
hg1797003
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7207
Supporting Variants
SamplesNA18507
Known GenesLINC00864, LOC439994, NUTM2A-AS1, NUTM2D
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)nssv9801
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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