A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323063



Internal ID20856179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204356697..204362747hg38UCSC Ensembl
chr1:204325825..204331875hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg386051
hg196051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057010
Samples
Known GenesPLEKHA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323063
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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