A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003851



Internal ID21913194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73093347..73093888hg38UCSC Ensembl
chr9:75708263..75708804hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003851
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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