A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582925



Internal ID21531442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80849273..80849457hg38UCSC Ensembl
chr7:80478589..80478773hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156212
SamplesHG00512
Known GenesSEMA3C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582925
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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