A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055021



Internal ID19144240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:59875368..59909042hg38UCSC Ensembl
Innerchr12:60269149..60302823hg19UCSC Ensembl
Innerchr12:58555416..58589090hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3833675
hg1933675
hg1833675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1509n100
Supporting Variantsnssv3523634
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)nsv1055021
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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