A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10007



Internal ID15542790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:18616812..19238847hg38UCSC Ensembl
Outerchr14:19393289..19826959hg19UCSC Ensembl
Outerchr14:18463289..18896959hg18UCSC Ensembl
Outerchr14:18463289..18896959hg17UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38622036
hg19433671
hg18433671
hg17433671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7248
Supporting Variants
SamplesNA18956
Known GenesBMS1P17, BMS1P18, LOC642426, POTEG
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)nssv10007
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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