A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440474



Internal ID21098027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91924473..92376273hg38UCSC Ensembl
chr9:94686755..95138555hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38451801
hg19451801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220474
Samples
Known GenesCENPP, IARS, LINC00475, LOC100128076, MIR3651, NOL8, ROR2, SNORA84, SPTLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440474
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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