A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332654



Internal ID20865828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15697862..15702442hg38UCSC Ensembl
chr1:16024357..16028937hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384581
hg194581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052291
Samples
Known GenesPLEKHM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332654
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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