A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141841



Internal ID21409468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:396986..397054hg38UCSC Ensembl
chr6:396986..397054hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569962
Supporting Variants
SamplesHG00512
Known GenesIRF4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141841
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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