A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408335



Internal ID21065888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52190159..52208193hg38UCSC Ensembl
chr6:52054957..52072991hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3818035
hg1918035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143996
Samples
Known GenesIL17A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408335
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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