A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322031



Internal ID20855140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203151999..203158860hg38UCSC Ensembl
chr1:203121127..203127988hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg386862
hg196862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056714
Samples
Known GenesADORA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322031
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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