A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503702



Internal ID22561643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18010486..18011605hg38UCSC Ensembl
chr6:18010717..18011836hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381120
hg191120
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845163
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503702
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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