A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963629



Internal ID22738564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113885171..113885171hg38UCSC Ensembl
chr10:115644930..115644930hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358592
Samples
Known GenesNHLRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963629
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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