A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515629



Internal ID20888990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74414900..74474227hg38UCSC Ensembl
chr18:72082135..72141462hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3859328
hg1959328
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197189
Samples
Known GenesFAM69C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515629
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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