A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873604



Internal ID22648552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:53365566..53370141hg38UCSC Ensembl
chr17:51442927..51447502hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384576
hg194576
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873604
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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