A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024908



Internal ID19114125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103011915..103072748hg38UCSC Ensembl
Innerchr6:103459790..103520623hg19UCSC Ensembl
Innerchr6:103566483..103627316hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3860834
hg1960834
hg1860834
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6116n100
Supporting Variantsnssv3649877
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)nsv1024908
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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