A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326336



Internal ID20859471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183549136..183549500hg38UCSC Ensembl
chr1:183518271..183518635hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054713
Samples
Known GenesSMG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326336
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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