A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454572



Internal ID21112125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63783901..63862600hg38UCSC Ensembl
chr9:68379635..68458334hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3878700
hg1978700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231811
Samples
Known GenesLOC642236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454572
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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