A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333566



Internal ID20866745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40375029..40406071hg38UCSC Ensembl
chr1:40840701..40871743hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3831043
hg1931043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060752
Samples
Known GenesSMAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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