A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029657



Internal ID19118875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25540570..25552131hg38UCSC Ensembl
Innerchr8:25398086..25409647hg19UCSC Ensembl
Innerchr8:25454003..25465564hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3811562
hg1911562
hg1811562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7149n100
Supporting Variantsnssv3685504, nssv3685505
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)nsv1029657
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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