A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv536



Internal ID15197965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26673441..26871078hg38UCSC Ensembl
Outerchr6:26673669..26838857hg19UCSC Ensembl
Outerchr6:26781648..26946836hg18UCSC Ensembl
Outerchr6:26781648..26946836hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38197638
hg19165189
hg18165189
hg17165189
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7378
Supporting Variants
SamplesNA19240
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)nssv536
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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