A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135930



Internal ID20702971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103223251..103250934hg38UCSC Ensembl
chr6:103671126..103698809hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3827684
hg1927684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619714
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135930
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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