A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225532



Internal ID20792572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121714286..121810937hg38UCSC Ensembl
chr7:121354340..121450991hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3896652
hg1996652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608051
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225532
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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