A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509737



Internal ID22567687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68735141..68756476hg38UCSC Ensembl
chr8:69647376..69668711hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3821336
hg1921336
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857112
Supporting Variants
Samples
Known GenesC8orf34
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509737
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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