A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401949



Internal ID21059502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115954739..115964577hg38UCSC Ensembl
chr5:115290436..115300274hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg389839
hg199839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125655
Samples
Known GenesAQPEP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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