A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872536



Internal ID22647476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80169573..80186249hg38UCSC Ensembl
chr17:78143372..78160048hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3816677
hg1916677
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479485
Samples
Known GenesCARD14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872536
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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