A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577684



Internal ID21526139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125387603..125390205hg38UCSC Ensembl
chr6:125708749..125711351hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382603
hg192603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152852
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577684
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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