A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963497



Internal ID22738432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107713728..107713728hg38UCSC Ensembl
chr9:110476009..110476009hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963497
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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