A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501589



Internal ID22559527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131324766..131331374hg38UCSC Ensembl
chr6:131645906..131652514hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg386609
hg196609
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844377
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501589
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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