A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6410



Internal ID15190768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97142683..97180452hg38UCSC Ensembl
Outerchr10:98902440..98940209hg19UCSC Ensembl
Outerchr10:98892430..98930199hg18UCSC Ensembl
Outerchr10:98892430..98930199hg17UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3837770
hg1937770
hg1837770
hg1737770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7506
Supporting Variants
SamplesNA12156
Known GenesARHGAP19-SLIT1, SLIT1
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)nssv6410
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