A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149426



Internal ID20716466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12300711..12348221hg38UCSC Ensembl
chr7:12340337..12387847hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3847511
hg1947511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617018
Supporting Variants
Samples
Known GenesVWDE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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