A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329770



Internal ID20862923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192163278..192163734hg38UCSC Ensembl
chr1:192132408..192132864hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18055088
Samples
Known GenesRGS18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329770
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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