A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523636



Internal ID18821917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:60559390..60626942hg38UCSC Ensembl
Innerchr12:60953171..61020723hg19UCSC Ensembl
Innerchr12:59239438..59306990hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3867553
hg1967553
hg1867553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038670
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)nssv3523636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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