A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138483



Internal ID20705523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130751975..130804547hg38UCSC Ensembl
chr6:131073120..131125687hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg3852573
hg1952568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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