A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540200



Internal ID20913492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38230542..38231082hg38UCSC Ensembl
chr21:39602464..39603004hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072334
Samples
Known GenesKCNJ15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540200
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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