A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207380



Internal ID22355774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38688367..38696205hg38UCSC Ensembl
chr4:38689988..38697826hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg387839
hg197839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314906
SamplesHG00732
Known GenesKLF3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207380
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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