A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869895



Internal ID22644830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39160163..39168201hg38UCSC Ensembl
chr17:37316416..37324454hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg388039
hg198039
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478231
Samples
Known GenesARL5C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869895
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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