A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985730



Internal ID20552770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95219440..95223022hg38UCSC Ensembl
chr10:96979197..96982779hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg383583
hg193583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450126
Supporting Variants
Samples
Known GenesC10orf129
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985730
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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