A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539700



Internal ID20912995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14222375..14222804hg38UCSC Ensembl
chr21:15594696..15595125hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069369
Samples
Known GenesRBM11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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