A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872009



Internal ID22646947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1728596..1729626hg38UCSC Ensembl
chr17:1631890..1632920hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381031
hg191031
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475544
Samples
Known GenesWDR81
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872009
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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