A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523827



Internal ID20897188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32739555..32740227hg38UCSC Ensembl
chr20:31327362..31328034hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067411
Samples
Known GenesCOMMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523827
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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