A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536035



Internal ID20909388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:23026399..23394477hg38UCSC Ensembl
chr21:24398721..24766798hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38368079
hg19368078
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071120
Samples
Known GenesD21S2088E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536035
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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