A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453982



Internal ID21111535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72203051..72204007hg38UCSC Ensembl
chr10:73962809..73963765hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983796
Samples
Known GenesASCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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