A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916955



Internal ID22692174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28844313..28844376hg38UCSC Ensembl
chr10:29133242..29133305hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916955
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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