A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135506



Internal ID20702546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112825525..112825985hg38UCSC Ensembl
chr6:113146727..113147187hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600992
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135506
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00094


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