A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076162



Internal ID21498156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76446317..76446317hg38UCSC Ensembl
chr11:76157361..76157361hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653256
Supporting Variants
SamplesNA19238
Known GenesC11orf30
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076162
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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