A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952531



Internal ID17301405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:26967064..26969063hg38UCSC Ensembl
Outerchr13:27541201..27543200hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998199
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952531
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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