A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452264



Internal ID21109817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129428101..129442100hg38UCSC Ensembl
chr9:132190380..132204379hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3814000
hg1914000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7948n223
Supporting Variantsnssv18221785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452264
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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