A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331092



Internal ID20864253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10183719..10202345hg38UCSC Ensembl
chr1:10243777..10262403hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3818627
hg1918627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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