A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324374



Internal ID20857500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240879753..240890107hg38UCSC Ensembl
chr1:241043053..241053407hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3810355
hg1910355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060143
Samples
Known GenesRGS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324374
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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