A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087009



Internal ID21434159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43128198..43128198hg38UCSC Ensembl
chr17:41280215..41280215hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652302
Supporting Variants
SamplesHG00731
Known GenesNBR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087009
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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