A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017677



Internal ID21927020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93615031..93615363hg38UCSC Ensembl
chr9:96377313..96377645hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585797
Samples
Known GenesPHF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017677
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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