A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510243



Internal ID22568193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92186427..92194425hg38UCSC Ensembl
chr8:93198655..93206653hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg387999
hg197999
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848326
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510243
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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