A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525219



Internal ID22394595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27388822..27388923hg38UCSC Ensembl
chr3:27430313..27430414hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307170, nssv14307169, nssv14307168
SamplesHG00731, HG00732, HG00733
Known GenesSLC4A7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525219
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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