A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154529



Internal ID20721569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42992741..42999709hg38UCSC Ensembl
chr7:43032340..43039308hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg386969
hg196969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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