A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154297



Internal ID21462278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107073197..107073250hg38UCSC Ensembl
chr6:107394401..107394454hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569081
Supporting Variants
SamplesHG02818
Known GenesBEND3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154297
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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