A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049266



Internal ID19138485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43801445..43827917hg38UCSC Ensembl
Innerchr10:44296893..44323365hg19UCSC Ensembl
Innerchr10:43616899..43643371hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3826473
hg1926473
hg1826473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513030, nssv3519125, nssv3519317
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049266
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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