A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362831



Internal ID22588500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72899232..72900230hg38UCSC Ensembl
chr10:74658990..74659988hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916070
Supporting Variants
Samples
Known GenesOIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362831
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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