A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155577



Internal ID21413570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123738520..123738688hg38UCSC Ensembl
chr6:124059665..124059833hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578230
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155577
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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