A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432538



Internal ID21090091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21085142..21099348hg38UCSC Ensembl
chr9:21085141..21099347hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3814207
hg1914207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432538
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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