A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437148



Internal ID21094701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92745693..92896447hg38UCSC Ensembl
chr9:95507975..95658729hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38150755
hg19150755
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219117
Samples
Known GenesANKRD19P, BICD2, ZNF484
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437148
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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