A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143432



Internal ID20710472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43702095..43703288hg38UCSC Ensembl
chr6:43669832..43671025hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381194
hg191194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396180
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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