A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340537



Internal ID20998090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:169571476..169578138hg38UCSC Ensembl
chr2:170427986..170434648hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg386663
hg196663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079974
Samples
Known GenesFASTKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340537
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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