A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076053



Internal ID21498177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7407348..7407678hg38UCSC Ensembl
chr11:7428579..7428909hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597184
Supporting Variants
SamplesNA19238
Known GenesSYT9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076053
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer