A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547004



Internal ID20920214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50050480..50053844hg38UCSC Ensembl
chr20:48667017..48670381hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg383365
hg193365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069037
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547004
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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