A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394574



Internal ID21052127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38907101..38908800hg38UCSC Ensembl
chr5:38907203..38908902hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130747
Samples
Known GenesOSMR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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