A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547698



Internal ID20920899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35578065..35578494hg38UCSC Ensembl
chr21:36950363..36950792hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072158
Samples
Known GenesLOC100506403
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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