A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579985



Internal ID21528470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:125097194..125134504hg38UCSC Ensembl
chr7:124737248..124774558hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3837311
hg1937311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152087
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579985
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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