A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999942



Internal ID17292894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:24802165..24816464hg38UCSC Ensembl
Outerchr20:24782801..24797100hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3814300
hg1914300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953006
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999942
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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