A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540854



Internal ID20914142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30319817..30320585hg38UCSC Ensembl
chr21:31692135..31692903hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069716
Samples
Known GenesKRTAP26-1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540854
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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