A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529037



Internal ID20902398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2581461..2587702hg38UCSC Ensembl
chr20:2562107..2568348hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386242
hg196242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067187
Samples
Known GenesTMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529037
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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