A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958860



Internal ID17307733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:37350859..37351118hg38UCSC Ensembl
Outerchr1:37816460..37816719hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005198
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958860
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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