A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15196710



Internal ID21335506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107557222..107557323hg38UCSC Ensembl
chr5:106892923..106893024hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3940541
Supporting Variants
SamplesHG002
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15196710
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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