A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522466



Internal ID20895827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81825071..81829369hg38UCSC Ensembl
chr17:79782947..79787245hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg384299
hg194299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039207
Samples
Known GenesFAM195B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522466
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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