A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6407



Internal ID15537457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:91406240..91445586hg38UCSC Ensembl
Outerchr10:93165997..93205343hg19UCSC Ensembl
Outerchr10:93155977..93195323hg18UCSC Ensembl
Outerchr10:93155977..93195323hg17UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3839347
hg1939347
hg1839347
hg1739347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7208
Supporting Variants
SamplesNA12156
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)nssv6407
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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