A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872935



Internal ID22647877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42635215..42645274hg38UCSC Ensembl
chr17:40787233..40797292hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3810060
hg1910060
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473803
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872935
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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