A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539348



Internal ID20912646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41012777..41013510hg38UCSC Ensembl
chr21:42384703..42385436hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539348
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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