A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999967



Internal ID17292919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:35226398..35227097hg38UCSC Ensembl
Outerchr20:33814201..33814900hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954028
Supporting Variants
SamplesBILGI_BIOE
Known GenesMMP24
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999967
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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