A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469522



Internal ID15187551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50516804..50687829hg38UCSC Ensembl
Innerchr10:52276564..52447589hg19UCSC Ensembl
Innerchr10:51946570..52117595hg18UCSC Ensembl
Innerchr10:51621167..51792192hg16UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38171026
hg19171026
hg18171026
hg16171026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672423, nssv1673843, nssv1675308
Samples
Known GenesSGMS1
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nsv469522
Frequency
Sample Size265
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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