A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999963



Internal ID17292915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:33442995..33443994hg38UCSC Ensembl
Outerchr20:32030801..32031800hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954023
Supporting Variants
SamplesBILGI_BIOE
Known GenesSNTA1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999963
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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