A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454758



Internal ID21112311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78718641..78743054hg38UCSC Ensembl
chr9:81333557..81357970hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3824414
hg1924414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190723
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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