A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449622



Internal ID21107175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64433301..64470000hg38UCSC Ensembl
chr9:69445719..69482418hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3836700
hg1936700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7779n223
Supporting Variantsnssv18231186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449622
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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