A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319492



Internal ID20852587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244368754..244378861hg38UCSC Ensembl
chr1:244532056..244542163hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3810108
hg1910108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059633
Samples
Known GenesC1orf100
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319492
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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