A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935302



Internal ID22710641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81125581..81125720hg38UCSC Ensembl
chr17:79099381..79099520hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382185
Samples
Known GenesAATK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935302
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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