A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444815



Internal ID21102368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129374729..129393793hg38UCSC Ensembl
chr9:132137008..132156072hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3819065
hg1919065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224543
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444815
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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