A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326726



Internal ID20859863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20703181..20703567hg38UCSC Ensembl
chr1:21029674..21030060hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199889
Samples
Known GenesKIF17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326726
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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