A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916572



Internal ID22691791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110912090..110912960hg38UCSC Ensembl
chr10:112671848..112672718hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363906
Samples
Known GenesBBIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916572
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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