A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9829



Internal ID15193208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:9293963..9472644hg38UCSC Ensembl
Outerchr12:9446559..9625240hg19UCSC Ensembl
Outerchr12:9337826..9516507hg18UCSC Ensembl
Outerchr12:9337826..9516507hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38178682
hg19178682
hg18178682
hg17178682
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7228
Supporting Variants
SamplesNA18507
Known GenesDDX12P, LOC642846
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)nssv9829
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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