A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432218



Internal ID21089771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1489600..1572987hg38UCSC Ensembl
chr9:1489600..1572987hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3883388
hg1983388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7541n223
Supporting Variantsnssv18175006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432218
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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