A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618955



Internal ID21811002
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 StatusS
Merged Variantsnsv6088907
Supporting Variants
Samples
Known GenesMAP3K14-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618955
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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