A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998199



Internal ID17291151
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 StatusS
Merged Variantsnsv952531
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998199
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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