A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386008



Internal ID21043561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138933999..138941972hg38UCSC Ensembl
chr4:139855153..139863126hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg387974
hg197974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386008
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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