A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499665



Internal ID20872888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35958730..35969137hg38UCSC Ensembl
chr17:34285734..34296151hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3810408
hg1910418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193169
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499665
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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