A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014198



Internal ID19103418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:66122469..66138702hg38UCSC Ensembl
Innerchr2:66349602..66365834hg19UCSC Ensembl
Innerchr2:66203106..66219338hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3816234
hg1916233
hg1816233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3577274
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)nsv1014198
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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