A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576660



Internal ID21525101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81433852..81433980hg38UCSC Ensembl
chr6:82143569..82143697hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155041
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576660
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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