A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532968



Internal ID20906329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77900552..77932125hg38UCSC Ensembl
chr17:75896634..75928207hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3831574
hg1931574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532968
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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