A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852524



Internal ID22627459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61717037..61720636hg38UCSC Ensembl
chr10:63476795..63480394hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452421
Samples
Known GenesC10orf107
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852524
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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