A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872402



Internal ID22647342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25822448..25822773hg38UCSC Ensembl
chr1:26148939..26149264hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367676
Samples
Known GenesLOC646471, MTFR1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872402
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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