A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452681



Internal ID21110234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13210947..13223140hg38UCSC Ensembl
chr10:13252947..13265140hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3812194
hg1912194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978525
Samples
Known GenesMCM10, UCMA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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