A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979938



Internal ID20546978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37969201..37977000hg38UCSC Ensembl
chr10:38258129..38265928hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450583
Supporting Variants
Samples
Known GenesZNF25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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