A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527148



Internal ID22396533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140993580..140995333hg38UCSC Ensembl
chr7:140693380..140695133hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381754
hg191754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14337044, nssv14337043
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527148
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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