A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373553



Internal ID21031106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4549862..4553051hg38UCSC Ensembl
chr4:4551589..4554778hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg383190
hg193190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117675
Samples
Known GenesSTX18-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373553
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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