A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439010



Internal ID22496880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84310752..84311086hg38UCSC Ensembl
chr8:85222987..85223321hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5909107
Supporting Variants
Samples
Known GenesRALYL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439010
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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