A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414634



Internal ID21072187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47969555..47985001hg38UCSC Ensembl
chr6:47937291..47952737hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3815447
hg1915447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143856
Samples
Known GenesPTCHD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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