A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925629



Internal ID22700856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:53988744..53992126hg38UCSC Ensembl
chr10:55748504..55751886hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg383383
hg193383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359316
Samples
Known GenesPCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925629
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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