A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373064



Internal ID21030617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187025201..187026600hg38UCSC Ensembl
chr3:186742989..186744388hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099564
Samples
Known GenesST6GAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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