A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903221



Internal ID22678386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75670891..75670957hg38UCSC Ensembl
chr6:76380607..76380673hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445005
Samples
Known GenesSENP6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903221
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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