A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330958



Internal ID20864118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86734411..86734859hg38UCSC Ensembl
chr1:87200094..87200542hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065549
Samples
Known GenesSH3GLB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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