A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9260



Internal ID15540211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:91400866..91446618hg38UCSC Ensembl
Outerchr10:93160623..93206375hg19UCSC Ensembl
Outerchr10:93150603..93196355hg18UCSC Ensembl
Outerchr10:93150603..93196355hg17UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3845753
hg1945753
hg1845753
hg1745753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7208
Supporting Variants
SamplesNA18517
Known GenesHECTD2, LOC100188947
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)nssv9260
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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