A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872547



Internal ID22647487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29556995..29563719hg38UCSC Ensembl
chr17:27884013..27890737hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg386725
hg196725
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477548
Samples
Known GenesABHD15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872547
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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