A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565822



Internal ID21514138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43067813..43068138hg38UCSC Ensembl
chr6:43035551..43035876hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152678
SamplesHG00731
Known GenesKLC4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565822
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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