A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047469



Internal ID19136688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65414695..65440777hg38UCSC Ensembl
Innerchr10:67174453..67200535hg19UCSC Ensembl
Innerchr10:66844459..66870541hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3826083
hg1926083
hg1826083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv880n100
Supporting Variantsnssv3707150
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)nsv1047469
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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