A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072554



Internal ID19320810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62547492..62552493hg38UCSC Ensembl
chr20:61144699..61149700hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg385002
hg195002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772349
SamplesKWP1
Known GenesC20orf166, C20orf166-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072554
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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