A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551305



Internal ID20924442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29756120..29756852hg38UCSC Ensembl
chr21:31128439..31129171hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072044
Samples
Known GenesGRIK1, GRIK1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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