A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506019



Internal ID20879294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5566942..5649447hg38UCSC Ensembl
chr16:5616943..5699448hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3882506
hg1982506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030187
Samples
Known GenesMIR8065
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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