A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710338



Internal ID19008619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:28845221..28901120hg38UCSC Ensembl
Innerchr12:28998154..29054053hg19UCSC Ensembl
Innerchr12:28889421..28945320hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3855900
hg1955900
hg1855900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042084
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)nssv3710338
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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