A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv468461



Internal ID15528526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:236440911..236618639hg38UCSC Ensembl
Innerchr1:236604211..236781939hg19UCSC Ensembl
Innerchr1:234670834..234848562hg18UCSC Ensembl
Innerchr1:232930252..233107980hg17UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38177729
hg19177729
hg18177729
hg17177729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv60n27
Supporting Variantsnssv543580
SamplesHGDP00021
Known GenesEDARADD, HEATR1, LGALS8, LGALS8-AS1
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)nsv468461
Frequency
Sample Size1557
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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