A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152025



Internal ID20719065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1050345..1052876hg38UCSC Ensembl
chr7:1089981..1092512hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382532
hg192532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604253
Supporting Variants
Samples
Known GenesC7orf50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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