A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449543



Internal ID21107096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108304441..108390712hg38UCSC Ensembl
chr9:111066721..111152992hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3886272
hg1986272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449543
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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