A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452892



Internal ID21110445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61425601..61428200hg38UCSC Ensembl
chr10:63185359..63187958hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982776
Samples
Known GenesTMEM26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452892
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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