A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397059



Internal ID21054612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148209007..148210440hg38UCSC Ensembl
chr5:147588570..147590003hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg381434
hg191434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125917
Samples
Known GenesSPINK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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