A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378195



Internal ID21035748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:129108001..129108444hg38UCSC Ensembl
chr4:130029156..130029599hg19UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110573
Samples
Known GenesC4orf33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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