A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495801



Internal ID20868996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38939100..38956317hg38UCSC Ensembl
chr17:37095353..37112570hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3817218
hg1917218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035313
Samples
Known GenesFBXO47
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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