A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335554



Internal ID20868747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169833313..169846766hg38UCSC Ensembl
chr1:169802454..169815907hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3813454
hg1913454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053334
Samples
Known GenesC1orf112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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