A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420696



Internal ID199791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25821664..25822766hg38UCSC Ensembl
chr1:26148155..26149257hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381103
hg191103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902419
Samples
Known GenesLOC646471, MTFR1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420696
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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