A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549803



Internal ID20922954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33604375..33618300hg38UCSC Ensembl
chr21:34976681..34990606hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3813926
hg1913926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071979
Samples
Known GenesCRYZL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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