A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529601



Internal ID20902962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63454521..63459190hg38UCSC Ensembl
chr17:61531882..61536551hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg384670
hg194670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037242
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529601
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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