A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088894



Internal ID21998127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6758470..6758470hg38UCSC Ensembl
chr17:6661789..6661789hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631085
Samples
Known GenesXAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088894
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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