A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328537



Internal ID20861685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75495601..75497100hg38UCSC Ensembl
chr1:75961286..75962785hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204425
Samples
Known GenesSLC44A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328537
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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