A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331311



Internal ID20864474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222131601..222135000hg38UCSC Ensembl
chr1:222304943..222308342hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv537n223
Supporting Variantsnssv18058646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331311
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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