A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547368



Internal ID20920571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36083098..36137209hg38UCSC Ensembl
chr21:37455396..37509507hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3854112
hg1954112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072179
Samples
Known GenesCBR3, CBR3-AS1, LOC100133286
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547368
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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