A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958134



Internal ID17307007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:30469457..30469681hg38UCSC Ensembl
Outerchr13:31043594..31043818hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004291
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958134
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