A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567897



Internal ID21516238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81343566..81343935hg38UCSC Ensembl
chr6:82053283..82053652hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140688
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567897
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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