A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983796



Internal ID20550836
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 StatusS
Merged Variantsnsv6453982
Supporting Variants
Samples
Known GenesASCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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