A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999915



Internal ID16946181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:3219555..3244454hg38UCSC Ensembl
Outerchr20:3200201..3225100hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3824900
hg1924900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952979
Supporting Variants
SamplesBILGI_BIOE
Known GenesITPA, SLC4A11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999915
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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