A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438286



Internal ID21095839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1618901..1641700hg38UCSC Ensembl
chr11:1640131..1662930hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3822800
hg1922800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186860
Samples
Known GenesKRTAP5-4, KRTAP5-5, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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