A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573191



Internal ID21521591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149626535..149628361hg38UCSC Ensembl
chr6:149947671..149949497hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381827
hg191827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157907
SamplesNA19238
Known GenesKATNA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573191
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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