A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315821



Internal ID20848895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101803918..101804678hg38UCSC Ensembl
chr1:102269474..102270234hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38761
hg19761
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050035
Samples
Known GenesOLFM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315821
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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