A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333680



Internal ID20866860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32087792..32097865hg38UCSC Ensembl
chr1:32553393..32563466hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3810074
hg1910074
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060428
Samples
Known GenesTMEM39B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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