A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842196



Internal ID22617131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17315913..17321437hg38UCSC Ensembl
chr5:17316022..17321546hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg385525
hg195525
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497714
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842196
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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