A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4899



Internal ID15196273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26681570..26858833hg38UCSC Ensembl
Outerchr6:26681798..26826612hg19UCSC Ensembl
Outerchr6:26789777..26934591hg18UCSC Ensembl
Outerchr6:26789777..26934591hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38177264
hg19144815
hg18144815
hg17144815
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7378
Supporting Variants
SamplesNA19129
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)nssv4899
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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