A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145186



Internal ID19279357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:7768978..7774878hg38UCSC Ensembl
Outerchr8:7626500..7632400hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg385901
hg195901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982270
SamplesKWS1
Known GenesFAM90A10P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145186
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer