A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237065



Internal ID20804105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:127940780..127973368hg38UCSC Ensembl
chr7:127580833..127613421hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3832589
hg1932589
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429196
Supporting Variants
Samples
Known GenesSND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237065
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00041


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