A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386141



Internal ID21043694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118879973..118880812hg38UCSC Ensembl
chr4:119801128..119801967hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108351
Samples
Known GenesSYNPO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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