A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042708



Internal ID19131927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132791887..132988338hg38UCSC Ensembl
Innerchr10:134605391..134801842hg19UCSC Ensembl
Innerchr10:134455381..134651832hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38196452
hg19196452
hg18196452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512492
Samples
Known GenesLOC399829, TTC40
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042708
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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