A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002035



Internal ID21911378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38206745..38206878hg38UCSC Ensembl
chr9:38206742..38206875hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002035
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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