A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154259



Internal ID20721299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120375654..120376090hg38UCSC Ensembl
chr7:120015708..120016144hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616523
Supporting Variants
Samples
Known GenesKCND2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00104


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