A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883761



Internal ID22658743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55456804..55460703hg38UCSC Ensembl
chr17:53534165..53538064hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv921n209
Supporting Variantsnssv17475131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883761
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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