A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849508



Internal ID22624443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22719113..22723557hg38UCSC Ensembl
chr10:23008042..23012486hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384445
hg194445
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849508
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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