A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865253



Internal ID22640188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64339345..64375829hg38UCSC Ensembl
chr10:66099105..66135589hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3836485
hg1936485
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865253
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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