A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10044



Internal ID15542753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:33612763..33624053hg38UCSC Ensembl
Outerchr15:33904964..33916254hg19UCSC Ensembl
Outerchr15:31692256..31703546hg18UCSC Ensembl
Outerchr15:31692256..31703546hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3811291
hg1911291
hg1811291
hg1711291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1483
Supporting Variants
SamplesNA18956
Known GenesRYR3
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)nssv10044
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer