A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501693



Internal ID20874930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41379456..41395148hg38UCSC Ensembl
chr17:39535708..39551400hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3815693
hg1915693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179369
Samples
Known GenesKRT31, KRT34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501693
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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