A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349984



Internal ID21007537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99338859..99349836hg38UCSC Ensembl
chr2:99955322..99966299hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3810978
hg1910978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090522
Samples
Known GenesEIF5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349984
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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