A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953399



Internal ID22728688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12002550..12002550hg38UCSC Ensembl
chr6:12002783..12002783hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953399
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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