A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427964



Internal ID206848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13557775..13575928hg38UCSC Ensembl
chr1:13884270..13902423hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3818154
hg1918154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17683829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427964
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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