A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363614



Internal ID21021167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25238806..25246214hg38UCSC Ensembl
chr4:25240428..25247836hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg387409
hg197409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113403
Samples
Known GenesPI4K2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363614
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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