A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553327



Internal ID20926435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63004755..63032849hg38UCSC Ensembl
chr20:61636107..61664201hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3828095
hg1928095
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203429
Samples
Known GenesBHLHE23, LOC63930
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553327
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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