A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355609



Internal ID21013162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16243487..16244163hg38UCSC Ensembl
chr4:16245110..16245786hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112459
Samples
Known GenesTAPT1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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