A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138950



Internal ID338134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157793641..157803391hg38UCSC Ensembl
chr1:157763431..157773181hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg389751
hg199751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890997
Samples
Known GenesFCRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138950
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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