A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439168



Internal ID21096721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72232053..72237386hg38UCSC Ensembl
chr10:73991811..73997144hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg385334
hg195334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983799
Samples
Known GenesANAPC16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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