A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330017



Internal ID20863171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39880735..39888431hg38UCSC Ensembl
chr1:40346407..40354103hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg387697
hg197697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060125
Samples
Known GenesTRIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330017
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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