A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17978275



Internal ID20545315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11672162..11684198hg38UCSC Ensembl
chr10:11714161..11726197hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3812037
hg1912037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438488
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17978275
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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