A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332842



Internal ID20866017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192170666..192171241hg38UCSC Ensembl
chr1:192139796..192140371hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18055089
Samples
Known GenesRGS18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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