A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036722



Internal ID19125941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26936975..26955043hg38UCSC Ensembl
Innerchr10:27225904..27243972hg19UCSC Ensembl
Innerchr10:27265910..27283978hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3818069
hg1918069
hg1818069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv695n100
Supporting Variantsnssv3707731, nssv3505231, nssv3512907, nssv3519297, nssv3505603, nssv3507598, nssv3519009
Samples
Known GenesLINC00202-1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036722
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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