A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9500



Internal ID15193128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:94978606..98502164hg38UCSC Ensembl
Outerchr13:95630860..99154418hg19UCSC Ensembl
Outerchr13:94428861..97952419hg18UCSC Ensembl
Outerchr13:94428861..97952419hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg383523559
hg193523559
hg183523559
hg173523559
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7246
Supporting Variants
SamplesNA18507
Known GenesABCC4, CLDN10, CLDN10-AS1, DNAJC3, DZIP1, FARP1, HS6ST3, IPO5, LINC00359, MBNL2, MIR3170, OXGR1, RAP2A, RNF113B, STK24, UGGT2
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)nssv9500
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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