A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036408



Internal ID19125627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7630029..7659414hg38UCSC Ensembl
Innerchr12:7782625..7812010hg19UCSC Ensembl
Innerchr12:7673892..7703277hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3829386
hg1929386
hg1829386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3708083
Samples
Known GenesAPOBEC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036408
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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