A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7185



Internal ID15552169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:172716549..172755600hg38UCSC Ensembl
Outerchr1:172685689..172724740hg19UCSC Ensembl
Outerchr1:170952312..170991363hg18UCSC Ensembl
Outerchr1:169417346..169456397hg17UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3839052
hg1939052
hg1839052
hg1739052
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3511
SamplesNA12878
Known Genes
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)nsv7185
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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