A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415026



Internal ID22472896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96787047..96794813hg38UCSC Ensembl
chr3:96505891..96513657hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg387767
hg197767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906228
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415026
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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