A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6629



Internal ID15190549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:40603261..40624071hg38UCSC Ensembl
Outerchr15:40895459..40916269hg19UCSC Ensembl
Outerchr15:38682751..38703561hg18UCSC Ensembl
Outerchr15:38682751..38703561hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3820811
hg1920811
hg1820811
hg1720811
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7263
Supporting Variants
SamplesNA12156
Known GenesCASC5
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)nssv6629
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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