A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414076



Internal ID22471946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195412946..195423699hg38UCSC Ensembl
chr3:195133675..195144428hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3810754
hg1910754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896842
Supporting Variants
Samples
Known GenesACAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414076
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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