A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378101



Internal ID21035654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138666160..138669015hg38UCSC Ensembl
chr4:139587314..139590169hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg382856
hg192856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378101
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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