A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040384



Internal ID19129603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:104964590..105815325hg38UCSC Ensembl
Innerchr10:106724348..107575083hg19UCSC Ensembl
Innerchr10:106714338..107565073hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38850736
hg19850736
hg18850736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507623
Samples
Known GenesSORCS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040384
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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