A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412606



Internal ID21070159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63355370..63363606hg38UCSC Ensembl
chr5:62651197..62659433hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg388237
hg198237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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