A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1526



Internal ID15199403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:47195685..47222285hg38UCSC Ensembl
Outerchr15:47487882..47514482hg19UCSC Ensembl
Outerchr15:45275174..45301774hg18UCSC Ensembl
Outerchr15:45275174..45301774hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3810224
hg1910224
hg1810224
hg1710224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5555, nssv6631
SamplesNA12156, NA19129
Known GenesSEMA6D
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)nsv1526
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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