A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv466418



Internal ID15526483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:71142654..71153632hg38UCSC Ensembl
Innerchr9:73757570..73768548hg19UCSC Ensembl
Innerchr9:72947390..72958368hg18UCSC Ensembl
Innerchr9:70987124..70998102hg17UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3810979
hg1910979
hg1810979
hg1710979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv541966
SamplesNINDS_174
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)nsv466418
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