A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861567



Internal ID22636502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50743416..50747535hg38UCSC Ensembl
chr10:52503176..52507295hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg384120
hg194120
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458742
Samples
Known GenesASAH2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861567
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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