A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359272



Internal ID21016825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16151790..16152695hg38UCSC Ensembl
chr4:16153413..16154318hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18111761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359272
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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