A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534778



Internal ID20908139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67654681..67667429hg38UCSC Ensembl
chr17:65650797..65663545hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3812749
hg1912749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037418
Samples
Known GenesPITPNC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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