A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529031



Internal ID22398424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155386878..155387021hg38UCSC Ensembl
chr7:155179573..155179716hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338746
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529031
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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