A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502952



Internal ID22560893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163163338..163166087hg38UCSC Ensembl
chr6:163584370..163587119hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg382750
hg192750
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844174
Supporting Variants
Samples
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502952
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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