A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1905



Internal ID15541188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:92355450..92378706hg38UCSC Ensembl
Outerchr10:94115207..94138463hg19UCSC Ensembl
Outerchr10:94105187..94128443hg18UCSC Ensembl
Outerchr10:94105187..94128443hg17UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3823257
hg1923257
hg1823257
hg1723257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7492
Supporting Variants
SamplesNA18555
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)nssv1905
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