A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443901



Internal ID21101454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127414158..127440063hg38UCSC Ensembl
chr9:130176437..130202342hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3825906
hg1925906
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225191
Samples
Known GenesZNF79
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443901
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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