A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328058



Internal ID20861203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:70413501..70427913hg38UCSC Ensembl
chr1:70879184..70893596hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3814413
hg1914413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062364
Samples
Known GenesCTH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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