A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148780



Internal ID21407649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110772889..110772889hg38UCSC Ensembl
chr6:111094092..111094092hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640393
Supporting Variants
SamplesHG00512
Known GenesCDK19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148780
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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