A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871434



Internal ID22646372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36029646..36029942hg38UCSC Ensembl
chr1:36495247..36495543hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376423
Samples
Known GenesAGO3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871434
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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