A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601781



Internal ID21550431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77376558..77376640hg38UCSC Ensembl
chr10:79136316..79136398hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071428
SamplesHG00732
Known GenesKCNMA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601781
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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