A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178045



Internal ID20745085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75566211..75571722hg38UCSC Ensembl
chr9:78181127..78186638hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385512
hg195512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444012
Supporting Variants
Samples
Known GenesMIR548H3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178045
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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