A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526127



Internal ID18824408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:125906783..125931200hg38UCSC Ensembl
Innerchr12:126391329..126415746hg19UCSC Ensembl
Innerchr12:124957282..124981699hg18UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3824418
hg1924418
hg1824418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037780
Supporting Variants
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)nssv3526127
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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