A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966102



Internal ID22741037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75155227..75155227hg38UCSC Ensembl
chr9:77770143..77770143hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430623
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966102
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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