A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453736



Internal ID21111289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93265661..93357205hg38UCSC Ensembl
chr9:96027943..96119487hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3891545
hg1991545
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223232
Samples
Known GenesC9orf129, WNK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453736
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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