A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886760



Internal ID22661749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75302232..75308301hg38UCSC Ensembl
chr17:73298313..73304382hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg386070
hg196070
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv925n209
Supporting Variantsnssv17476426, nssv17476425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886760
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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