A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317128



Internal ID20850212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27203522..27209966hg38UCSC Ensembl
chr1:27530013..27536457hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386445
hg196445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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