A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076011



Internal ID21415569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7331215..7331215hg38UCSC Ensembl
chr11:7352446..7352446hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654092
Supporting Variants
SamplesHG00731
Known GenesSYT9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076011
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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