A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433331



Internal ID22491201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3924208..3925897hg38UCSC Ensembl
chr6:3924442..3926131hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381690
hg191690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888586
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433331
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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