A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436129



Internal ID214751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:196683980..196685343hg38UCSC Ensembl
chr1:196653110..196654473hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16894175
Samples
Known GenesCFH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436129
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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