A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450318



Internal ID21107871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73258859..73261037hg38UCSC Ensembl
chr9:75873775..75875953hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382179
hg192179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450318
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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