A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195703



Internal ID22345836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1409001..1419400hg38UCSC Ensembl
chr4:1402789..1413188hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14311704, nssv14311706, nssv14311705, nssv14311710, nssv14311707, nssv14311708, nssv14311703, nssv14311702, nssv14311709
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195703
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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