A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315635



Internal ID20848706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:193280240..193284083hg38UCSC Ensembl
chr1:193249370..193253213hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg383844
hg193844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18055262
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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