A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001445



Internal ID21910788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135887656..135887771hg38UCSC Ensembl
chr9:138779502..138779617hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584603
Samples
Known GenesCAMSAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001445
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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