A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325277



Internal ID20858408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150699524..150702996hg38UCSC Ensembl
chr1:150672000..150675472hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383473
hg193473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052985
Samples
Known GenesHORMAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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