A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435829



Internal ID21093382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106035945..106041397hg38UCSC Ensembl
chr9:108798226..108803678hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg385453
hg195453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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