A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098197



Internal ID22007430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35604068..35604068hg38UCSC Ensembl
chr17:33931087..33931087hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383834
hg193834
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635131
Samples
Known GenesAP2B1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098197
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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