A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129245



Internal ID21447106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24906364..24906364hg38UCSC Ensembl
chr4:24907986..24907986hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604940
Supporting Variants
SamplesHG00732
Known GenesCCDC149
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129245
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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