A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953305



Internal ID22728594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46109871..46109871hg38UCSC Ensembl
chr6:46077608..46077608hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434104
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953305
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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