A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532732



Internal ID20906093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77120545..77125073hg38UCSC Ensembl
chr17:75116627..75121155hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg384529
hg194529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038978
Samples
Known GenesSEC14L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532732
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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