A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445952



Internal ID21103505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72041269..72058460hg38UCSC Ensembl
chr10:73801027..73818218hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3817192
hg1917192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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