A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043378



Internal ID19132597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95095609..95116252hg38UCSC Ensembl
Innerchr10:96855366..96876009hg19UCSC Ensembl
Innerchr10:96845356..96865999hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3820644
hg1920644
hg1820644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv960n100
Supporting Variantsnssv3509884
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)nsv1043378
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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