A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007345



Internal ID19096564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:67643093..67752962hg38UCSC Ensembl
Innerchr2:67870225..67980094hg19UCSC Ensembl
Innerchr2:67723729..67833598hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38109870
hg19109870
hg18109870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3730859
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)nsv1007345
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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