A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749883



Internal ID21388763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222377080..222377877hg38UCSC Ensembl
chr1:222550422..222551219hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433047
Supporting Variants
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749883
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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