A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952997



Internal ID17301871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:20353457..20358856hg38UCSC Ensembl
Outerchr20:20334101..20339500hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999933
SamplesBILGI_BIOE
Known GenesC20orf26
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952997
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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