A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906082



Internal ID22681277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53119753..53119825hg38UCSC Ensembl
chr6:52984551..52984623hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906082
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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