A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502953



Internal ID22560894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163258863..163261909hg38UCSC Ensembl
chr6:163679895..163682941hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg383047
hg193047
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844799
Supporting Variants
Samples
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502953
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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