A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576012



Internal ID21524446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:415127..415183hg38UCSC Ensembl
chr7:455093..455149hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140213
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576012
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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