A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17981392



Internal ID20548432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30289574..30292987hg38UCSC Ensembl
chr10:30578503..30581916hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg383414
hg193414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436940
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17981392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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