A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903657



Internal ID22678826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158701175..158701356hg38UCSC Ensembl
chr6:159122207..159122388hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428915
Samples
Known GenesSYTL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903657
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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