A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415306



Internal ID22473176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39310860..39368788hg38UCSC Ensembl
chr3:39352351..39410279hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3857929
hg1957929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900268
Supporting Variants
Samples
Known GenesCCR8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415306
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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