A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827



Internal ID15544721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37061793..37112129hg38UCSC Ensembl
Outerchr10:37350721..37401057hg19UCSC Ensembl
Outerchr10:37390727..37441063hg18UCSC Ensembl
Outerchr10:37390727..37441063hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3850337
hg1950337
hg1850337
hg1750337
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7201
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)nssv827
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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