A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7200



Internal ID15552186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:24492511..24521895hg38UCSC Ensembl
Outerchr10:24781440..24810824hg19UCSC Ensembl
Outerchr10:24821446..24850830hg18UCSC Ensembl
Outerchr10:24821446..24850830hg17UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3829385
hg1929385
hg1829385
hg1729385
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3868
SamplesNA12878
Known GenesKIAA1217
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)nsv7200
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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