A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006456



Internal ID21915799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124883159..124883247hg38UCSC Ensembl
chr9:127645438..127645526hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578011
Samples
Known GenesGOLGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006456
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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