A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601070



Internal ID21549714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32061587..32061648hg38UCSC Ensembl
chr12:32214521..32214582hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092641
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601070
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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