A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138499



Internal ID337683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149656000..149664293hg38UCSC Ensembl
chr1:149627610..149635895hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg388294
hg198286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891097
Samples
Known GenesLINC00869
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138499
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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