A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3522870



Internal ID22392294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105908614..105908722hg38UCSC Ensembl
chr7:105549060..105549168hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14336866, nssv14336867, nssv14336864, nssv14336861, nssv14336869, nssv14336868, nssv14336863, nssv14336865, nssv14336862
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3522870
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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