A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925717



Internal ID22700944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4654489..4655149hg38UCSC Ensembl
chr10:4696681..4697341hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366504
Samples
Known GenesLINC00704
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925717
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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