A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024924



Internal ID19114141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61288172..61350771hg38UCSC Ensembl
Innerchr6:61886428..61949543hg19UCSC Ensembl
Innerchr6:61944387..62007502hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3862600
hg1963116
hg1863116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5983n100
Supporting Variantsnssv3657577
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)nsv1024924
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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