A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507254



Internal ID22565202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63219897..63238955hg38UCSC Ensembl
chr6:63929802..63948860hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3819059
hg1919059
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507254
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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