A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7351



Internal ID15205666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:12111102..12859846hg38UCSC Ensembl
Outerchr3:12152602..12901345hg19UCSC Ensembl
Outerchr3:12127602..12876345hg18UCSC Ensembl
Outerchr3:12127602..12876345hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38748745
hg19748744
hg18748744
hg17748744
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10335
SamplesNA18956
Known GenesC3orf83, CAND2, MKRN2, PPARG, RAF1, RPL32, SNORA7A, SYN2, TIMP4, TMEM40, TSEN2
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)nsv7351
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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