A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000012



Internal ID17292964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:62305045..62338544hg38UCSC Ensembl
Outerchr20:60880101..60913600hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3833500
hg1933500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953301
Supporting Variants
SamplesBILGI_BIOE
Known GenesADRM1, LAMA5, MIR4758
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000012
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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