A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080808



Internal ID21990041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41177934..41177934hg38UCSC Ensembl
chr17:39334186..39334186hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635017
Samples
Known GenesKRTAP4-2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080808
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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