A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067671



Internal ID20634712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50601162..50627590hg38UCSC Ensembl
chr20:49217699..49244127hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3826429
hg1926429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552841
Supporting Variants
Samples
Known GenesFAM65C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067671
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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