A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152655



Internal ID20719695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12703819..12887693hg38UCSC Ensembl
chr7:12743444..12927318hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38183875
hg19183875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618298
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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