A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041805



Internal ID19131024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:92865002..92939866hg38UCSC Ensembl
Innerchr10:94624759..94699623hg19UCSC Ensembl
Innerchr10:94614739..94689603hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3874865
hg1974865
hg1874865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv954n100
Supporting Variantsnssv3508654
Samples
Known GenesEXOC6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041805
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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