A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360629



Internal ID22586298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18812860..18812909hg38UCSC Ensembl
chr10:19101789..19101838hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5908885
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360629
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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