A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026093



Internal ID19115310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60683016..61103618hg38UCSC Ensembl
Innerchr6:57650763..58071365hg19UCSC Ensembl
Innerchr6:57758722..58179324hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38420603
hg19420603
hg18420603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5971n100
Supporting Variantsnssv3657523
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)nsv1026093
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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