A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749632



Internal ID21384142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42869748..42871533hg38UCSC Ensembl
chr6:42837486..42839271hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381786
hg191786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434970
Supporting Variants
SamplesBTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749632
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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