A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998235



Internal ID17291187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:66226269..66232668hg38UCSC Ensembl
Outerchr13:66800401..66806800hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951896
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998235
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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