A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607306



Internal ID20980377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149504379..149504993hg38UCSC Ensembl
chr6:149825515..149826129hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141872
Samples
Known GenesPPIL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607306
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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