A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579013



Internal ID21527488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:186176907..186177042hg38UCSC Ensembl
chr1:186146039..186146174hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062535
SamplesHG03125
Known GenesHMCN1, MIR548F1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579013
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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