A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328791



Internal ID20861941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106954281..106954781hg38UCSC Ensembl
chr1:107496903..107497403hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328791
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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