A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526356



Internal ID20899717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57532021..57533568hg38UCSC Ensembl
chr17:55609382..55610929hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381548
hg191548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187097
Samples
Known GenesMSI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526356
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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