A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852648



Internal ID22627583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:105258729..105276308hg38UCSC Ensembl
chr10:107018487..107036066hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3817580
hg1917580
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453218
Samples
Known GenesSORCS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852648
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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