A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330241



Internal ID20863397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209536701..209543600hg38UCSC Ensembl
chr1:209710046..209716945hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330241
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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