A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875212



Internal ID22650169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74977234..74984504hg38UCSC Ensembl
chr17:72973329..72980599hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg387271
hg197271
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875212
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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