A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035871



Internal ID19125090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:119526435..119556257hg38UCSC Ensembl
Innerchr12:119964240..119994062hg19UCSC Ensembl
Innerchr12:118448623..118478445hg18UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg3829823
hg1929823
hg1829823
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3526082
Samples
Known GenesCCDC60
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035871
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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