A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215572



Internal ID22361858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149061566..149062147hg38UCSC Ensembl
chr7:148758658..148759239hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338543, nssv14338544, nssv14338545
SamplesNA19239, HG00732, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215572
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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