A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022375



Internal ID19111593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61274104..61350771hg38UCSC Ensembl
Innerchr6:61886428..61963609hg19UCSC Ensembl
Innerchr6:61944387..62021568hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3876668
hg1977182
hg1877182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5983n100
Supporting Variantsnssv3657579, nssv3657578
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)nsv1022375
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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