A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427181



Internal ID22485051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157706348..157706398hg38UCSC Ensembl
chr6:158127380..158127430hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906609
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427181
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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