A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447132



Internal ID21104685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88423473..88430917hg38UCSC Ensembl
chr9:91038388..91045832hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg387445
hg197445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223468
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447132
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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