A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036830



Internal ID19126049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:28913688..28938205hg38UCSC Ensembl
Innerchr12:29066621..29091138hg19UCSC Ensembl
Innerchr12:28957888..28982405hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3824518
hg1924518
hg1824518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505508
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036830
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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