A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6912



Internal ID15190266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:234097479..234151390hg18UCSC Ensembl
Outerchr2:234214740..234268651hg17UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg1853912
hg1753912
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7336
Supporting Variants
SamplesNA12156
Known GenesUSP40
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)nssv6912
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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