A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868971



Internal ID22643906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77011014..77015054hg38UCSC Ensembl
chr17:75007096..75011136hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg384041
hg194041
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868971
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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