A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14338183



Internal ID22225680
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229160
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14338183
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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