A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394114



Internal ID21051667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10696517..10700696hg38UCSC Ensembl
chr5:10696629..10700808hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg384180
hg194180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124166
Samples
Known GenesDAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394114
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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