A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436776



Internal ID21094329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66261301..66275500hg38UCSC Ensembl
chr9:42246196..42259708hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3814200
hg1913513
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436776
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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