A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9264



Internal ID15193529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:26857093..26877823hg38UCSC Ensembl
Outerchr1:27183584..27204314hg19UCSC Ensembl
Outerchr1:27056171..27076901hg18UCSC Ensembl
Outerchr1:26867726..26888456hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3816852
hg1916852
hg1816852
hg1716852
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7535
Supporting Variants
SamplesNA18517
Known GenesSFN
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)nssv9264
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