A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040158



Internal ID19129377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:19579836..19683692hg38UCSC Ensembl
Innerchr12:19732770..19836626hg19UCSC Ensembl
Innerchr12:19624037..19727893hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38103857
hg19103857
hg18103857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1400n100
Supporting Variantsnssv3511807
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)nsv1040158
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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