A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444394



Internal ID22502264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26201826..26206365hg38UCSC Ensembl
chr7:26241446..26245985hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg384540
hg194540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914876
Supporting Variants
Samples
Known GenesCBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444394
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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