A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452596



Internal ID21110149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33602474..33744291hg38UCSC Ensembl
chr9:33602472..33744289hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38141818
hg19141818
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224299
Samples
Known GenesANXA2P2, LOC101929688, PTENP1, PTENP1-AS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452596
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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