A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032414



Internal ID19121636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:61876687..61948817hg38UCSC Ensembl
Innerchr8:62789246..62861376hg19UCSC Ensembl
Innerchr8:62951800..63023930hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3872131
hg1972131
hg1872131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757281
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)nsv1032414
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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