A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138125



Internal ID337307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50889526..50908036hg38UCSC Ensembl
chr1:51355198..51373708hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3818511
hg1918511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902961
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138125
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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