A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399166



Internal ID21056719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53035839..53037588hg38UCSC Ensembl
chr6:52900637..52902386hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg381750
hg191750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144043
Samples
Known GenesICK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399166
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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