A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10917



Internal ID15539505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:34502488..34557782hg38UCSC Ensembl
Outerchr14:34971694..35026988hg19UCSC Ensembl
Outerchr14:34041445..34096739hg18UCSC Ensembl
Outerchr14:34041445..34096739hg17UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3855295
hg1955295
hg1855295
hg1755295
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7251
Supporting Variants
SamplesNA15510
Known GenesEAPP
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)nssv10917
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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