A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154861



Internal ID20721901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22788665..22794581hg38UCSC Ensembl
chr7:22828284..22834200hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385917
hg195917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613892
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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