A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361327



Internal ID21018880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17613193..17623128hg38UCSC Ensembl
chr4:17614816..17624751hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg389936
hg199936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114202
Samples
Known GenesMED28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361327
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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