A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399766



Internal ID21057319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2764501..2766000hg38UCSC Ensembl
chr6:2764735..2766234hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224845
Samples
Known GenesWRNIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399766
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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