A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229160



Internal ID22371094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128152012..128152120hg38UCSC Ensembl
chr7:127792064..127792172hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8744n152
Supporting Variantsnssv14338182, nssv14338183
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229160
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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