A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539277



Internal ID20912578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32580219..32584929hg38UCSC Ensembl
chr21:33952529..33957239hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg384711
hg194711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071939
Samples
Known GenesTCP10L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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