A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012335



Internal ID19101553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:19000803..19057636hg38UCSC Ensembl
Innerchr2:19182076..19257397hg19UCSC Ensembl
Innerchr2:19045557..19120878hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3856834
hg1975322
hg1875322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3578982
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)nsv1012335
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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