A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184294



Internal ID20751334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73909571..73919230hg38UCSC Ensembl
chr9:76524487..76534146hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg389660
hg199660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439772
Supporting Variants
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184294
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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