A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045702



Internal ID18788233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103385173..103553473hg38UCSC Ensembl
Innerchr10:105144930..105313230hg19UCSC Ensembl
Innerchr10:105134920..105303220hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38168301
hg19168301
hg18168301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv966n100
Supporting Variantsnssv3515473
Samples
Known GenesCALHM1, CALHM2, CALHM3, MIR1307, NEURL1, PDCD11, TAF5, USMG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045702
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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