A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526128



Internal ID18824409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:125906783..125932360hg38UCSC Ensembl
Innerchr12:126391329..126416906hg19UCSC Ensembl
Innerchr12:124957282..124982859hg18UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg3825578
hg1925578
hg1825578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051188
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)nssv3526128
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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