A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086601



Internal ID21272403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:154960553..154965312hg38UCSC Ensembl
Innerchr6:155281687..155286446hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg384760
hg194760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112262
Supporting Variants
Samplessample177
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086601
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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