A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3894



Internal ID15538621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:98533429..98552796hg38UCSC Ensembl
Outerchr10:100293186..100312553hg19UCSC Ensembl
Outerchr10:100283176..100302543hg18UCSC Ensembl
Outerchr10:100283176..100302543hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3819368
hg1919368
hg1819368
hg1719368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7209
Supporting Variants
SamplesNA12878
Known GenesHPSE2
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)nssv3894
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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