A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17977160



Internal ID20544200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100154307..100154639hg38UCSC Ensembl
chr10:101914064..101914396hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440044
Supporting Variants
Samples
Known GenesERLIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17977160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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