A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057781



Internal ID21967014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57187322..57192471hg38UCSC Ensembl
chr20:55762378..55767527hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg385150
hg195150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631330
Samples
Known GenesBMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057781
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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