A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044286



Internal ID19133505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130499509..130525581hg38UCSC Ensembl
Innerchr10:132297773..132323845hg19UCSC Ensembl
Innerchr10:132187763..132213835hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3826073
hg1926073
hg1826073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514063
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)nsv1044286
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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