A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436017



Internal ID22493887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98067676..98069371hg38UCSC Ensembl
chr8:99079904..99081599hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg381696
hg191696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915281
Supporting Variants
Samples
Known GenesC8orf47
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436017
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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