A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952520



Internal ID17301394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:18943761..18966160hg38UCSC Ensembl
Outerchr13:19517901..19540300hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3822400
hg1922400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998187
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952520
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