A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146380



Internal ID20713420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74468616..74474530hg38UCSC Ensembl
chr6:75178332..75184246hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg385915
hg195915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408128
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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