A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095676



Internal ID22004909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2035402..2035402hg38UCSC Ensembl
chr17:1938696..1938696hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626730
Samples
Known GenesDPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095676
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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