A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5297



Internal ID15196712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:72037700..72073268hg38UCSC Ensembl
Outerchr10:73797458..73833026hg19UCSC Ensembl
Outerchr10:73467464..73503032hg18UCSC Ensembl
Outerchr10:73467464..73503032hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3835569
hg1935569
hg1835569
hg1735569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7204
Supporting Variants
SamplesNA19129
Known GenesSPOCK2
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)nssv5297
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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