A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372905



Internal ID21030458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4689434..4695528hg38UCSC Ensembl
chr4:4691161..4697255hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg386095
hg196095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117175
Samples
Known GenesSTX18-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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