A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419268



Internal ID198405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27959303..27961887hg38UCSC Ensembl
chr1:28285814..28288398hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382585
hg192585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901243
Samples
Known GenesXKR8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419268
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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