A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835602



Internal ID22610537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:30930398..30934641hg38UCSC Ensembl
chr3:30971890..30976133hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg384244
hg194244
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490656, nssv17491591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835602
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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