A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508461



Internal ID18806742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:28241369..28445085hg38UCSC Ensembl
Innerchr12:28394302..28598018hg19UCSC Ensembl
Innerchr12:28285569..28489285hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38203717
hg19203717
hg18203717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043710
Supporting Variants
Samples
Known GenesCCDC91
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3508461
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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