A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156840



Internal ID20723880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19921569..19923858hg38UCSC Ensembl
chr7:19961192..19963481hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg382290
hg192290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606391
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156840
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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