A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv464631



Internal ID15524696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89928234..90080467hg38UCSC Ensembl
Innerchr7:89557548..89709781hg19UCSC Ensembl
Innerchr7:89395484..89547717hg18UCSC Ensembl
Innerchr7:89202199..89354432hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38152234
hg19152234
hg18152234
hg17152234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv825n27
Supporting Variantsnssv540520
SamplesNINDS_149
Known Genes
MethodSNP array
AnalysisAn HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives.
PlatformNot reported
Comments
ReferenceItsara_et_al_2009
Pubmed ID19166990
Accession Number(s)nsv464631
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer