A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878082



Internal ID22653047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8171435..8178047hg38UCSC Ensembl
chr17:8074753..8081365hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg386613
hg196613
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476524
Samples
Known GenesTMEM107
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878082
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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