A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884607



Internal ID22659590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42856996..42859720hg38UCSC Ensembl
chr1:43322667..43325391hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg382725
hg192725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387047
Samples
Known GenesLOC339539
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884607
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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