A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579012



Internal ID21527487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240207686..240207817hg38UCSC Ensembl
chr1:240370986..240371117hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063551
SamplesHG03009
Known GenesFMN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579012
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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