A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040338



Internal ID19129557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120072164..120113427hg38UCSC Ensembl
Innerchr10:121831676..121872939hg19UCSC Ensembl
Innerchr10:121821666..121862929hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3841264
hg1941264
hg1841264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507570
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)nsv1040338
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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