A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053225



Internal ID21962459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42583693..42945183hg38UCSC Ensembl
chr19:43087845..43449335hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38361491
hg19361491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617654
Samples
Known GenesCEACAM8, LIPE-AS1, LOC100289650, PSG1, PSG10P, PSG3, PSG6, PSG7, PSG8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053225
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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