A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330170



Internal ID20863325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:76593799..76594189hg38UCSC Ensembl
chr1:77059484..77059874hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063147
Samples
Known GenesST6GALNAC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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