A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036914



Internal ID18779445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:85807925..85878715hg38UCSC Ensembl
Innerchr12:86201703..86272493hg19UCSC Ensembl
Innerchr12:84725834..84796624hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3870791
hg1970791
hg1870791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1539n100
Supporting Variantsnssv3524767
Samples
Known GenesNTS, RASSF9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036914
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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