A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936649



Internal ID22712006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37050106..37050158hg38UCSC Ensembl
chr17:35407404..35407456hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387591
Samples
Known GenesAATF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936649
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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