A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326338



Internal ID20859473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240917001..240925200hg38UCSC Ensembl
chr1:241080301..241088500hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060145
Samples
Known GenesRGS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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