A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538159



Internal ID20911482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57210991..57211419hg38UCSC Ensembl
chr20:55786047..55786475hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070465
Samples
Known GenesBMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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