A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887766



Internal ID22662762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42495326..42501135hg38UCSC Ensembl
chr6:42463064..42468873hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385810
hg195810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887766
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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