A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431870



Internal ID22489740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28983460..28989460hg38UCSC Ensembl
chr6:28951237..28957237hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900940
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431870
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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