A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732704



Internal ID20508629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21064717..21065815hg38UCSC Ensembl
chr20:21045358..21046456hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732704
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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