A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575644



Internal ID21524074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85062032..85062088hg38UCSC Ensembl
chr6:85771750..85771806hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140534
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575644
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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