A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500256



Internal ID22558193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102974365..102983964hg38UCSC Ensembl
chr6:103422240..103431839hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843623
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500256
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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