A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162415



Internal ID20729455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99375374..99381140hg38UCSC Ensembl
chr7:98972997..98978763hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385767
hg195767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604941
Supporting Variants
Samples
Known GenesARPC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162415
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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