A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578690



Internal ID21770733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92250608..92250677hg38UCSC Ensembl
chr9:95012890..95012959hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004114
Supporting Variants
Samples
Known GenesIARS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578690
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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