A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508472



Internal ID20881773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34654919..34656394hg38UCSC Ensembl
chr17:32981938..32983413hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381476
hg191476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508472
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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