A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035772



Internal ID19124991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:58314825..58338272hg38UCSC Ensembl
Innerchr12:58708608..58732055hg19UCSC Ensembl
Innerchr12:56994875..57018322hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3823448
hg1923448
hg1823448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523608
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)nsv1035772
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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