A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013924



Internal ID19103143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34434857..34512096hg38UCSC Ensembl
Innerchr2:34659924..34737163hg19UCSC Ensembl
Innerchr2:34513428..34590667hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3877240
hg1977240
hg1877240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3758n100
Supporting Variantsnssv3728040, nssv3580976, nssv3580973, nssv3580971, nssv3580974, nssv3580969, nssv3580972, nssv3728038, nssv3580975, nssv3580978, nssv3580965, nssv3580966, nssv3580967, nssv3580968, nssv3580970, nssv3580979, nssv3728039, nssv3728041, nssv3580977, nssv3728037
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)nsv1013924
Frequency
Sample Size11257
Observed Gain20
Observed Loss0
Observed Complex0
Frequencyn/a


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