A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842



Internal ID15204006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13911858..13939698hg38UCSC Ensembl
Outerchr10:13953858..13981698hg19UCSC Ensembl
Outerchr10:13993864..14021704hg18UCSC Ensembl
Outerchr10:13993864..14021704hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3827841
hg1927841
hg1827841
hg1727841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8445
SamplesNA12156
Known GenesFRMD4A
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)nsv5842
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