A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935728



Internal ID22711073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37034914..37040470hg38UCSC Ensembl
chr17:35392211..35397767hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg385557
hg195557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381274
Samples
Known GenesAATF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935728
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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