A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749101



Internal ID21391250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184111846..184112573hg38UCSC Ensembl
chr1:184080980..184081707hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433000
Supporting Variants
SamplesNB12
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749101
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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