A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570419



Internal ID21518784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107976856..107976947hg38UCSC Ensembl
chr7:107617301..107617392hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143023
SamplesHG00732
Known GenesLAMB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570419
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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