A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517988



Internal ID20891349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72683741..72690523hg38UCSC Ensembl
chr17:70679880..70686662hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg386783
hg196783
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195850
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517988
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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