A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17980312



Internal ID20547352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4395501..4397900hg38UCSC Ensembl
chr10:4437693..4440092hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442791
Supporting Variants
Samples
Known GenesLINC00703
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17980312
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01226


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