A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983580



Internal ID20550620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7906370..7952733hg38UCSC Ensembl
chr10:7948333..7994696hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3846364
hg1946364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441853
Supporting Variants
Samples
Known GenesTAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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