A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953692



Internal ID22728971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91347963..91347963hg38UCSC Ensembl
chr9:94110245..94110245hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438156
Samples
Known GenesAUH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953692
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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