A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505844



Internal ID22563788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4569247..4572919hg38UCSC Ensembl
chr6:4569481..4573153hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg383673
hg193673
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505844
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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