A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048906



Internal ID19138125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121672001..121692680hg38UCSC Ensembl
Innerchr10:123431515..123452194hg19UCSC Ensembl
Innerchr10:123421505..123442184hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3820680
hg1920680
hg1820680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv983n100
Supporting Variantsnssv3519713
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)nsv1048906
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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