A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18075367



Internal ID20642408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10970107..10977593hg38UCSC Ensembl
chr2:11110233..11117719hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg387487
hg197487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6348773
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18075367
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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