A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10633



Internal ID15542165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:85802464..85838445hg38UCSC Ensembl
Outerchr8:86814693..86850674hg19UCSC Ensembl
Outerchr8:86884264..86919765hg18UCSC Ensembl
Outerchr8:86884264..86919765hg17UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3835982
hg1935982
hg1835502
hg1735502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6285
Supporting Variants
SamplesNA18956
Known GenesREXO1L2P
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)nssv10633
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