A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140977



Internal ID19265556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62799759..62799809hg38UCSC Ensembl
Outerchr9:66455583..66455633hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3992487
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140977
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