A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907401



Internal ID22682609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43797993..43798260hg38UCSC Ensembl
chr6:43765730..43765997hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907401
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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