A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998197



Internal ID16944463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:26049663..26052462hg38UCSC Ensembl
Outerchr13:26623801..26626600hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952529
Supporting Variants
SamplesBILGI_BIOE
Known GenesSHISA2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998197
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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