A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319220



Internal ID20852312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192318497..192319173hg38UCSC Ensembl
chr1:192287627..192288303hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18055477
Samples
Known GenesRGS21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319220
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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