A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154773



Internal ID20721813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17908256..17934017hg38UCSC Ensembl
chr7:17947879..17973640hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3825762
hg1925762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613883
Supporting Variants
Samples
Known GenesSNX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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