A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316421



Internal ID20849500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11737555..11738958hg38UCSC Ensembl
chr1:11797612..11799015hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381404
hg191404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051843
Samples
Known GenesAGTRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316421
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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