A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446730



Internal ID22504600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26208607..26212023hg38UCSC Ensembl
chr7:26248227..26251643hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg383417
hg193417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924058
Supporting Variants
Samples
Known GenesCBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446730
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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