A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008929



Internal ID20575971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41003395..41003533hg38UCSC Ensembl
chr13:41577531..41577669hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493075
Supporting Variants
Samples
Known GenesELF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03076


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