A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577829



Internal ID21526286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124961618..124961698hg38UCSC Ensembl
chr7:124601672..124601752hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156316
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577829
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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