A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335000



Internal ID20868190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187106016..187151577hg38UCSC Ensembl
chr1:187075148..187120709hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3845562
hg1945562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335000
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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