A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042652



Internal ID19131871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:29941897..29980387hg38UCSC Ensembl
Innerchr12:30094830..30133320hg19UCSC Ensembl
Innerchr12:29986097..30024587hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3838491
hg1938491
hg1838491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512418
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)nsv1042652
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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