A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037692



Internal ID18780223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44712577..44876329hg38UCSC Ensembl
Innerchr10:45208025..45371777hg19UCSC Ensembl
Innerchr10:44528031..44691783hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38163753
hg19163753
hg18163753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv729n100
Supporting Variantsnssv3505263
Samples
Known GenesTMEM72-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037692
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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