A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510291



Internal ID20883608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62450701..62451500hg38UCSC Ensembl
chr16:62484605..62485404hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510291
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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