A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551740



Internal ID20924872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39893563..39894089hg38UCSC Ensembl
chr21:41265488..41266014hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072670
Samples
Known GenesPCP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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