A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578074



Internal ID21526536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152385313..152385643hg38UCSC Ensembl
chr7:152082398..152082728hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143077
SamplesNA19238
Known GenesKMT2C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578074
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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