A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999904



Internal ID17292856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1177457..1189056hg38UCSC Ensembl
Outerchr20:1158101..1169700hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3811600
hg1911600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952968
Supporting Variants
SamplesBILGI_BIOE
Known GenesTMEM74B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999904
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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