A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149509



Internal ID20716549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106976201..106984200hg38UCSC Ensembl
chr7:106616646..106624645hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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