A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876686



Internal ID22651647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28579555..28579901hg38UCSC Ensembl
chr1:28906067..28906413hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358743
Samples
Known GenesSNHG12, SNORA61
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876686
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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