A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512144



Internal ID20885474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21404292..21691678hg38UCSC Ensembl
chr17:21307604..21566608hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38287387
hg19259005
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3034n223
Supporting Variantsnssv18194395
Samples
Known GenesC17orf51, KCNJ12, KCNJ18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512144
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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