A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499026



Internal ID20872242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37525695..37532397hg38UCSC Ensembl
chr17:35885798..35892499hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386703
hg196702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181791
Samples
Known GenesSYNRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499026
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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