A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431605



Internal ID210377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156383511..156383762hg38UCSC Ensembl
chr1:156353302..156353553hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890896
Samples
Known GenesRHBG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431605
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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