A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935257



Internal ID22710596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77469891..77469966hg38UCSC Ensembl
chr17:75465973..75466048hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381173
Samples
Known GenesSEPT9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935257
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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