A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2410



Internal ID15200287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:111486928..111510250hg38UCSC Ensembl
Outerchr1:112029550..112052872hg19UCSC Ensembl
Outerchr1:111831073..111854395hg18UCSC Ensembl
Outerchr1:111741592..111764914hg17UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3813370
hg1913370
hg1813370
hg1713370
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9568
SamplesNA18507
Known GenesADORA3
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)nsv2410
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