A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521033



Internal ID20894394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33347440..33355335hg38UCSC Ensembl
chr20:31935246..31943141hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg387896
hg197896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067440
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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