A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868601



Internal ID22643536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157579352..157579686hg38UCSC Ensembl
chr1:157549142..157549476hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352081
Samples
Known GenesFCRL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868601
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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