A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320667



Internal ID20853767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77947623..77947964hg38UCSC Ensembl
chr1:78413308..78413649hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063235
Samples
Known GenesFUBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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