A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315685



Internal ID20848757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212924333..212930446hg38UCSC Ensembl
chr1:213097675..213103788hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg386114
hg196114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315685
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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