A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326195



Internal ID20859329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118240701..118263400hg38UCSC Ensembl
chr1:118783324..118806023hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3822700
hg1922700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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