A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7174



Internal ID15205471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:25265296..25391733hg38UCSC Ensembl
Outerchr1:25591787..25718224hg19UCSC Ensembl
Outerchr1:25464374..25590811hg18UCSC Ensembl
Outerchr1:25337102..25463540hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38126438
hg19126438
hg18126438
hg17126439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9251, nssv9262
SamplesNA18517
Known GenesRHCE, RHD, TMEM50A
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)nsv7174
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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