A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501758



Internal ID22559697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137363976..137369072hg38UCSC Ensembl
chr6:137685113..137690209hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg385097
hg195097
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843768
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501758
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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