A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950811



Internal ID17299685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:13488476..13490875hg38UCSC Ensembl
Outerchr7:13528101..13530500hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997615
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950811
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