A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944662



Internal ID22720130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74877356..74881650hg38UCSC Ensembl
chr17:72873485..72877780hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg384295
hg194296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381006
Samples
Known GenesFADS6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944662
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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