A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7197



Internal ID15205496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:4942134..4986839hg38UCSC Ensembl
Outerchr10:4984326..5029031hg19UCSC Ensembl
Outerchr10:4974326..5019031hg18UCSC Ensembl
Outerchr10:4974326..5019031hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3844706
hg1944706
hg1844706
hg1744706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3858
SamplesNA12878
Known GenesAKR1C1
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)nsv7197
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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