A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418786



Internal ID21076339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:700235..1471770hg38UCSC Ensembl
chr9:700235..1471770hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38771536
hg19771536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220558
Samples
Known GenesDMRT1, DMRT2, DMRT3, KANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418786
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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