A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535785



Internal ID20909138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14627801..14629300hg38UCSC Ensembl
chr21:16000122..16001621hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068643
Samples
Known GenesLOC388813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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