A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438157



Internal ID21095710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132712327..132713257hg38UCSC Ensembl
chr9:135587714..135588644hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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