A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045804



Internal ID19135023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121673138..121696088hg38UCSC Ensembl
Innerchr10:123432652..123455602hg19UCSC Ensembl
Innerchr10:123422642..123445592hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3822951
hg1922951
hg1822951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv984n100
Supporting Variantsnssv3506247, nssv3506092
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)nsv1045804
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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