A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956088



Internal ID22731280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85238009..85238009hg38UCSC Ensembl
chr6:85947727..85947727hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439850
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956088
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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