A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1679



Internal ID15546242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:95379796..95411891hg38UCSC Ensembl
Outerchr15:95923025..95955120hg19UCSC Ensembl
Outerchr15:93724029..93756124hg18UCSC Ensembl
Outerchr15:93724029..93756124hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg387344
hg197344
hg187344
hg177344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6647
SamplesNA12156
Known Genes
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)nsv1679
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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