A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15750588



Internal ID21388811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49160331..49161063hg38UCSC Ensembl
chr3:49197764..49198496hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434061
Supporting Variants
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15750588
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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