A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088907



Internal ID21998140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45262544..45262544hg38UCSC Ensembl
chr17:43339911..43339911hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618955
Samples
Known GenesMAP3K14-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088907
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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