A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871304



Internal ID22646241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31862645..31868972hg38UCSC Ensembl
chr17:30189664..30195991hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg386328
hg196328
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478121
Samples
Known GenesUTP6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871304
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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