A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856243



Internal ID22631178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18196941..18200040hg38UCSC Ensembl
chrUn_gl000212:25693..28792hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv504n209
Supporting Variantsnssv17456126, nssv17450017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856243
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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