A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319865



Internal ID20852962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156615656..156617389hg38UCSC Ensembl
chr1:156585448..156587181hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381734
hg191734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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