A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546136



Internal ID20919355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39781080..39781749hg38UCSC Ensembl
chr21:41153007..41153676hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072654
Samples
Known GenesIGSF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546136
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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