A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443173



Internal ID21100726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63291201..63373600hg38UCSC Ensembl
chr9:67246173..67328572hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3882400
hg1982400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7758n223
Supporting Variantsnssv18235667
Samples
Known GenesAQP7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443173
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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