A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083412



Internal ID21266659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27419335..27469919hg38UCSC Ensembl
Innerchr7:27458954..27509538hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3850585
hg1950585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111750
Supporting Variants
Samplessample100
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083412
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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