A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935169



Internal ID22710507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45080534..45080627hg38UCSC Ensembl
chr17:43157902..43157995hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388299
Samples
Known GenesNMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935169
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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