A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439097



Internal ID21096650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63542501..63600300hg38UCSC Ensembl
chr9:68138235..68196034hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3857800
hg1957800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7767n223
Supporting Variantsnssv18235647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439097
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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