A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142884



Internal ID20709924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34204630..34216705hg38UCSC Ensembl
chr6:34172407..34184482hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3812076
hg1912076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401068
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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