A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153117



Internal ID21424690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96712371..96712526hg38UCSC Ensembl
chr6:97160247..97160402hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566056
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153117
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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