A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979859



Internal ID20546899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36701901..36709084hg38UCSC Ensembl
chr10:36990829..36998012hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg387184
hg197184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437195
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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