A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326201



Internal ID20859335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241099971..241104380hg38UCSC Ensembl
chr1:241263271..241267680hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg384410
hg194410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059062
Samples
Known GenesRGS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326201
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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