A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138914



Internal ID338098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149957136..149957487hg38UCSC Ensembl
chr1:149929048..149929399hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891127
Samples
Known GenesOTUD7B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138914
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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