A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851342



Internal ID22626277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60392091..60415895hg38UCSC Ensembl
chr10:62151849..62175653hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3823805
hg1923805
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454303
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851342
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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